Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Deseret Medical, Inc. · Predicate Candidate Screening
20 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
64 daysmedian FDA review time
233 days90th percentile
20clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K913027 | VESSEL DILATOR | Deseret Medical, Inc. | 1991-11-27 | 141 | 0 |
| K904648 | SAFE SYTE I.V. CATHETER PLACEMENT UNIT | Deseret Medical, Inc. | 1990-12-14 | 64 | 0 |
| K904121 | VIALON OBTURATOR | Deseret Medical, Inc. | 1990-11-08 | 63 | 0 |
| K904122 | INSYTE-A ARTERIAL CATHETERIZATION UNIT | Deseret Medical, Inc. | 1990-10-04 | 28 | 0 |
| K900116 | DESERET OPTIMA INTRAVASCULAR CATHETER | Deseret Medical, Inc. | 1990-06-18 | 160 | 0 |
| K895735 | DESERET MULTILUMEN SUBCLAVIAN CATHETER | Deseret Medical, Inc. | 1990-05-18 | 233 | 0 |
| K895734 | DESERET INTRAVASCULAR CATHETER | Deseret Medical, Inc. | 1990-04-09 | 195 | 0 |
| K894033 | DISPOSABLE CATHETER PRESSURE TRANSDUCER | Deseret Medical, Inc. | 1989-10-17 | 133 | 0 |
| K893406 | DESERET PRN ADAPTER | Deseret Medical, Inc. | 1989-06-22 | 51 | 0 |
| K882798 | MULTIFLO ADAPTER | Deseret Medical, Inc. | 1988-07-18 | 12 | 0 |
| K882797 | LUER-LOK MULTIFLO ADAPTER | Deseret Medical, Inc. | 1988-07-18 | 12 | 0 |
| K881695 | DESERET SUBCLAVIAN HEMODIALYSIS CATHETER | Deseret Medical, Inc. | 1988-06-23 | 65 | 0 |
| K874165 | DISPOSABLE CATHETER PRESSURE TRANSDUCER | Deseret Medical, Inc. | 1988-06-09 | 240 | 0 |
| K874582 | DESERET SPLITTABLE CATHETER | Deseret Medical, Inc. | 1987-12-29 | 50 | 0 |
| K833657 | ANGIO-SET INTRAVENOUS CATH. SET | Deseret Medical, Inc. | 1983-12-27 | 70 | 0 |
| K832558 | RELEASE OF ETHYLENE OXIDE-STERILIZ. DEV | Deseret Medical, Inc. | 1983-11-28 | 119 | 0 |
| K813595 | PARKE-DAVIS AEGIS ABOSRBENT SPONGES | Deseret Medical, Inc. | 1982-01-18 | 21 | 0 |
| K811343 | HUMERAL FRACTURE CAST BRACE | Deseret Medical, Inc. | 1981-05-28 | 16 | 0 |
| K801650 | DESERET EMBOLECTOMY/THROMBECTOMY CATH. | Deseret Medical, Inc. | 1980-08-04 | 17 | 0 |
| K790327 | ANGIO-FLO | Deseret Medical, Inc. | 1979-02-26 | 10 | 0 |
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