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Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account

V. Mueller O.V. Baxter Healthcare Corp. · Predicate Candidate Screening

41 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

35 daysmedian FDA review time
149 days90th percentile
41clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K803292FIELD SUCTION DISSECTORV. Mueller O.V. Baxter Healthcare Corp.1981-01-29300
K792383KELMAN DIPSTICKV. Mueller O.V. Baxter Healthcare Corp.1979-12-11150
K771197NORTON ENDOTRACHEALV. Mueller O.V. Baxter Healthcare Corp.1977-08-16460
K771302PFISTER-SCHWARTZ STONE RETRIEVERV. Mueller O.V. Baxter Healthcare Corp.1977-08-02180
K770959BOUGIE, FILIFORM, JACKSONV. Mueller O.V. Baxter Healthcare Corp.1977-06-14180
K770280CORD, ELECTROSURGICAL-STERILE & DISPOS.V. Mueller O.V. Baxter Healthcare Corp.1977-04-15600
K760851CONVERSE ALTAR RETRACTORV. Mueller O.V. Baxter Healthcare Corp.1977-03-101460
K761242TEFLON COATED RESECTOSCOPE SHEATHV. Mueller O.V. Baxter Healthcare Corp.1976-12-1630
K760273LITHOTRITEV. Mueller O.V. Baxter Healthcare Corp.1976-12-061370
K760172OBTURATOR, VISUALV. Mueller O.V. Baxter Healthcare Corp.1976-12-021490
K760173BRIDGE, SHORT DEFLECTINGV. Mueller O.V. Baxter Healthcare Corp.1976-12-021490
K760179SHEATH, CYSTOURETHROSCOPE W/ OBTURATORV. Mueller O.V. Baxter Healthcare Corp.1976-12-021490
K760180FORCEPS, GRASPINGV. Mueller O.V. Baxter Healthcare Corp.1976-12-021490
K760182SHEATH, RESECTOSCOPEV. Mueller O.V. Baxter Healthcare Corp.1976-12-021490
K760183OBTURATOR, DEFLECTINGV. Mueller O.V. Baxter Healthcare Corp.1976-12-021490
K760184ELEMENT, WORKINGV. Mueller O.V. Baxter Healthcare Corp.1976-12-021490
K760189STOPCOCK, WATERLINEV. Mueller O.V. Baxter Healthcare Corp.1976-12-021490
K760791COOLEY ANGLED SCISSOR - 1MM PROBE POINTV. Mueller O.V. Baxter Healthcare Corp.1976-11-11350
K760792SCISSOR - 1.5MM PROBE POINT, ANGLEDV. Mueller O.V. Baxter Healthcare Corp.1976-11-11350
K760850PARKES HUMP GAUGE STRAIGHT 7 (18 CM)V. Mueller O.V. Baxter Healthcare Corp.1976-11-03190
K760579INSTRUMENT RACK FOR DAWSON-YUHL INSTR.V. Mueller O.V. Baxter Healthcare Corp.1976-11-02600
K760847FELDSTEIN BLEPHAROPLASTY CLIP SHARP PV. Mueller O.V. Baxter Healthcare Corp.1976-11-02180
K760848FELDSTEIN BLEPHAROPLASTY CLIP RECTANGUV. Mueller O.V. Baxter Healthcare Corp.1976-11-02180
K760849FELDSTEIN BLEPHAROSTOMY CLIP SQUAREV. Mueller O.V. Baxter Healthcare Corp.1976-11-02180
K760357SKIN CLIP SYSTEM, DISPOSABLE (AVLOX ICI)V. Mueller O.V. Baxter Healthcare Corp.1976-10-27860
K760715FLEXIBLE CUTTING SCISSORSV. Mueller O.V. Baxter Healthcare Corp.1976-10-21260
K760717FLEXIBLE BIOPSY FORCEPSV. Mueller O.V. Baxter Healthcare Corp.1976-10-21260
K760178ELECTRODE, CUTTING LOOPV. Mueller O.V. Baxter Healthcare Corp.1976-10-151010
K760716FLEXIBLE FOREIGN BODY FORCEPSV. Mueller O.V. Baxter Healthcare Corp.1976-10-15200
K760793ADAPTER FOR ELLIK EVACUATORV. Mueller O.V. Baxter Healthcare Corp.1976-10-1580
K760174ADAPTER, RESECTOSCOPEV. Mueller O.V. Baxter Healthcare Corp.1976-08-30550
K760175DRAPE, TRANSURETHRAL RESECTION (TUR)V. Mueller O.V. Baxter Healthcare Corp.1976-08-30550
K760176FLOORSTAND, FIBER OPTIC LIGHT SOURCEV. Mueller O.V. Baxter Healthcare Corp.1976-08-30550
K760177TELESCOPE, RIGID ENDOSCOPEV. Mueller O.V. Baxter Healthcare Corp.1976-08-30550
K760274TIP, RUBBER, PERFORATEDV. Mueller O.V. Baxter Healthcare Corp.1976-08-30390
K760185SCISSORS, MICRO IRIS STRAIGHTV. Mueller O.V. Baxter Healthcare Corp.1976-08-04290
K760186DISSECTOR, TROUTMAN CORNEALV. Mueller O.V. Baxter Healthcare Corp.1976-08-04290
K760187KNIFE, TROUTMAN CORNEAL SMALLV. Mueller O.V. Baxter Healthcare Corp.1976-08-04290
K760188SCISSORS, MICRO IRIS CURVEDV. Mueller O.V. Baxter Healthcare Corp.1976-08-04290
K760190SCISSORS, IRIS STRAIGHTV. Mueller O.V. Baxter Healthcare Corp.1976-08-04290
K760191KNIFE, TROUTMAN CORNEAL LARGEV. Mueller O.V. Baxter Healthcare Corp.1976-08-04290

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda