Deseret Medical, Inc.
FDA 510(k) medical device clearances.
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.