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Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Technicare Corp. — Predicate Candidate Screening

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

47 daysmedian FDA review time
100 days90th percentile
32clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K854340TECHNICARE 720 HPS CT SCANNERTechnicare Corp.1985-11-15180
K852089SATURN NUCLEAR MEDICINE COMPUTER SYSTEMTechnicare Corp.1985-07-18660
K844293AUTO DII MULTI FREQUENCYTechnicare Corp.1985-02-131000
K844247ULTRASONIC SCANNER CALIBRATION & TEST PHANTOMSTechnicare Corp.1985-01-23830
K843716NUCLEAR 700 MEDICINE MECHANICAL POSIT-Technicare Corp.1984-12-17840
K842777AUTOFOCUS DUAL ELEMENT PROBETechnicare Corp.1984-11-291360
K841817TECHNICARE 248 SL & 260SLTechnicare Corp.1984-08-171080
K840860CENTAURI CT SCANNERTechnicare Corp.1984-05-22880
K840540TECHNICARE MODEL 330Technicare Corp.1984-05-09910
K834486TECHNICARE 280Technicare Corp.1984-04-131280
K840390TECHNICARE MODEL 1047Technicare Corp.1984-02-21220
K837499AUTOSECTORTechnicare Corp.1983-06-10320
K837430AUTO D OPTIONTechnicare Corp.1983-05-18190
K837046AUTOFOCUS PROBE FOR USE WITH ULTRASOUND AUTOSECTOR SYSTEMTechnicare Corp.1983-04-01810
K827644DELTASCAN HPS CT SCANNERTechnicare Corp.1982-07-22280
K827610ULTRASOUND AUTO SECTOR CARDIAC MODULETechnicare Corp.1982-07-20350
K827652TECHNICARE ULTRASOUND AUTO SECTOR B-SCAN ARM OPTIONTechnicare Corp.1982-07-20220
K827571MOBILE DIGITAL RECEPTORTechnicare Corp.1982-07-09370
K827501MODEL 580 DIGITAL RADIOGRAPHY SYSTEMTechnicare Corp.1982-06-09300
K827378DIAGNOSTIC X-RAY HV GENERATORTechnicare Corp.1982-05-19290
K827122DELTA PLAN II RADIATION THERAPY PLANNING SYSTEMTechnicare Corp.1982-03-31540
K820310DELTA PLAN II RADIATION THERAPY PLANTechnicare Corp.1982-03-31540
K813596AUTO SECTOR MCUTechnicare Corp.1982-03-25870
K827036AUTO SECTOR MCUTechnicare Corp.1982-03-25870
K813196IMAGE ANALYSIS CENTERTechnicare Corp.1981-12-29470
K813073OMEGA 500 RECTANGULAR FIELD CAMERA W/SCTechnicare Corp.1981-12-08360
K812743FETAL VITABILITY TM MODETechnicare Corp.1981-11-16480
K812410DELTASCAN 2060 CT SCANNERTechnicare Corp.1981-10-02420
K811931NEEDLE GUIDE ATTACHMENTTechnicare Corp.1981-08-18430
K801948DIGITAL SUBTRACTION RADIOGRAPHY SYSTEMTechnicare Corp.1980-09-26420
K801056EDP 1200 ULTRASONIC B-SCANNERTechnicare Corp.1980-06-04290
K800892NUCLEAR STRESS TABLE (NST-1)Technicare Corp.1980-05-14260

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