Deseret Medical, Inc.
Deseret Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 1979, most recent 1991.
Top product codes for Deseret Medical, Inc.
Recent clearances by Deseret Medical, Inc.
- K913027 — VESSEL DILATOR
- K904648 — SAFE SYTE I.V. CATHETER PLACEMENT UNIT
- K904121 — VIALON OBTURATOR
- K904122 — INSYTE-A ARTERIAL CATHETERIZATION UNIT
- K900116 — DESERET OPTIMA INTRAVASCULAR CATHETER
- K895735 — DESERET MULTILUMEN SUBCLAVIAN CATHETER
- K895734 — DESERET INTRAVASCULAR CATHETER
- K894033 — DISPOSABLE CATHETER PRESSURE TRANSDUCER
- K893406 — DESERET PRN ADAPTER
- K882797 — LUER-LOK MULTIFLO ADAPTER
- K882798 — MULTIFLO ADAPTER
- K881695 — DESERET SUBCLAVIAN HEMODIALYSIS CATHETER
- K874165 — DISPOSABLE CATHETER PRESSURE TRANSDUCER
- K874582 — DESERET SPLITTABLE CATHETER
- K833657 — ANGIO-SET INTRAVENOUS CATH. SET
- K832558 — RELEASE OF ETHYLENE OXIDE-STERILIZ. DEV
- K813595 — PARKE-DAVIS AEGIS ABOSRBENT SPONGES
- K811343 — HUMERAL FRACTURE CAST BRACE
- K801650 — DESERET EMBOLECTOMY/THROMBECTOMY CATH.
- K790327 — ANGIO-FLO
Data sourced from openFDA. This site is unofficial and independent of the FDA.