Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Sheridan Catheter Corp. — Predicate Candidate Screening
39 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
39 daysmedian FDA review time
95 days90th percentile
39clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K922894 | LAZER-TRACH TRACHEAL TUBE | Sheridan Catheter Corp. | 1993-05-07 | 325 | 0 |
| K897046 | LASER RESISTANT TRACHEAL TUBE | Sheridan Catheter Corp. | 1990-03-23 | 95 | 0 |
| K890823 | ACCESSORY TO CLINICAL ELECTRONIC THERMOMETER | Sheridan Catheter Corp. | 1989-05-05 | 77 | 0 |
| K884765 | CLINICAL ELECTRONIC THERMOMETERS | Sheridan Catheter Corp. | 1989-02-16 | 94 | 0 |
| K882918 | KIM NASO-INTESTINAL TUBE | Sheridan Catheter Corp. | 1988-12-05 | 146 | 0 |
| K882127 | CLINICAL ELECTRONIC THERMOMETERS | Sheridan Catheter Corp. | 1988-08-04 | 76 | 0 |
| K881368 | CLINICAL ELECTONIC THERMOMETERS | Sheridan Catheter Corp. | 1988-07-13 | 22 | 0 |
| K881293 | SHERIDAN ELECTROSURGERY PROTECTION FILTER | Sheridan Catheter Corp. | 1988-06-16 | 80 | 0 |
| K881873 | INTRODUCTION/DRAINAGE CATHETER & ACCESS | Sheridan Catheter Corp. | 1988-05-18 | 15 | 0 |
| K880960 | NDYAG LASER TRACHEAL TUBE | Sheridan Catheter Corp. | 1988-04-29 | 52 | 0 |
| K875226 | ESOPHAGEAL OBTURATOR/TRACHEAL TUBE | Sheridan Catheter Corp. | 1988-01-19 | 28 | 0 |
| K874295 | ESOPHAGEAL STETHOSCOPE W/ELECTRICAL CONDUCTORS | Sheridan Catheter Corp. | 1987-11-24 | 35 | 0 |
| K872616 | BELL/MCKAY TRACHEAL TUBE | Sheridan Catheter Corp. | 1987-08-10 | 35 | 0 |
| K864468 | TRACHEOBRONCHIAL SUCTION CATHETER | Sheridan Catheter Corp. | 1987-01-06 | 55 | 0 |
| K863302 | MODIFIED FOLEY CATHETER | Sheridan Catheter Corp. | 1986-10-03 | 39 | 0 |
| K863142 | THORACIC CATHETER (CHEST DRAINAGE TUBE) | Sheridan Catheter Corp. | 1986-08-29 | 14 | 0 |
| K862347 | ENDOTRACHEAL TUBE, ACCESSORY | Sheridan Catheter Corp. | 1986-07-11 | 21 | 1 |
| K861541 | SHERIDAN - YSI/ECG SONATEMP (TM) | Sheridan Catheter Corp. | 1986-06-16 | 53 | 0 |
| K861454 | END TIDAL CO2 TUBE | Sheridan Catheter Corp. | 1986-05-06 | 18 | 0 |
| K860802 | TRACHEOBRONCHIAL SUCTION CATHETER | Sheridan Catheter Corp. | 1986-04-02 | 29 | 0 |
| K860105 | SPIRAL-FLEX | Sheridan Catheter Corp. | 1986-03-04 | 50 | 0 |
| K860176 | LARYNGECTOMY TUBE, CUFFED | Sheridan Catheter Corp. | 1986-01-27 | 10 | 0 |
| K851857 | UROLOGICAL CATHETER & ACCESSORIES FOLEY CATHETER | Sheridan Catheter Corp. | 1985-07-15 | 80 | 0 |
| K851671 | GASTROINTESTINAL TUBE | Sheridan Catheter Corp. | 1985-06-14 | 52 | 0 |
| K851856 | TRACHEAL/BRONCHIAL DIFFERENTIAL VENTILATION TUBE | Sheridan Catheter Corp. | 1985-05-23 | 27 | 3 |
| K850964 | DOUBLE-SWIVEL CONNECTOR | Sheridan Catheter Corp. | 1985-05-14 | 67 | 5 |
| K850244 | CLINICAL ELECTRONIC THERMOMETERS | Sheridan Catheter Corp. | 1985-04-04 | 72 | 0 |
| K844746 | TRACHEAL TUBE W/AIRWAY INTUBATOR | Sheridan Catheter Corp. | 1985-01-14 | 39 | 0 |
| K844296 | TRACHEAL TUBE, REINFORCED, CUFFED | Sheridan Catheter Corp. | 1984-12-04 | 28 | 0 |
| K842635 | SHERIDAN/ENDO-PAK | Sheridan Catheter Corp. | 1984-07-25 | 16 | 0 |
| K842558 | SHERIDAN/INTENSA TUBE | Sheridan Catheter Corp. | 1984-07-11 | 9 | 0 |
| K841098 | SHERIDAN YSI/SONATEMP | Sheridan Catheter Corp. | 1984-04-30 | 48 | 0 |
| K834562 | ENTERNAL FEEDING TUBE | Sheridan Catheter Corp. | 1984-02-13 | 47 | 0 |
| K834463 | LARYNGOTRACHEAL TOPICAL ANES. APPLI | Sheridan Catheter Corp. | 1984-01-13 | 24 | 0 |
| K832196 | SHERIDAN/LEVI-A-SUMP | Sheridan Catheter Corp. | 1983-10-14 | 99 | 0 |
| K832865 | FLEX BUBBLE TUBING | Sheridan Catheter Corp. | 1983-09-29 | 37 | 0 |
| K832773 | SHERI-I-SLIP INTUBATING STYLET | Sheridan Catheter Corp. | 1983-09-12 | 27 | 0 |
| K830218 | SHERIDAN/ESOPHAGEAL STETHOSCOPE | Sheridan Catheter Corp. | 1983-03-09 | 44 | 0 |
| K822082 | SHERIDAN/HVT,CF, UNCUFFED | Sheridan Catheter Corp. | 1982-08-10 | 29 | 27 |
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