Precision Medical, Inc.
Precision Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 2018, with 1 FDA device recall on record.
Top product codes for Precision Medical, Inc.
FDA recalls by Precision Medical, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Precision Medical, Inc.
- K173807 — Accu O2 Oxygen Analyzer
- K140179 — EASY GO VAC
- K103563 — PRECISION PORTABLE OXYGEN CONCENTRATION MODEL 4150
- K103324 — PRECISION LIQUID OXYGEN SYSTEM
- K090781 — HELIO2 BLENDER
- K072348 — PRECISION OXYGEN CONCENTRATOR
- K063096 — PRECISION OXYGEN MONITOR
- K053232 — PRECISION BLENDER
- K051691 — MINIMATE COMPRESSOR
- K041122 — PRECISION LIQUID OXYGEN SYSTEM
- K032018 — EASY PULSE II OXYGEN CONSERVER
- K001412 — PM 1800 CONSERVING DEVICE
- K971749 — EASYGO ASPIRATOR
- K944479 — PM3300 INTERMITTENT VACUUM
- K941818 — PM9000 VAC TRAP
- K942350 — CAREPAK
- K930509 — PM PUMP COMPRESSOR
- K932006 — 1500 SERIES REGULATOR
- K932494 — PM PUMP ASPIRATOR
- K922817 — PM3000 & PM3100 VACUUM REGULATOR
- K923324 — PRECISION MIST COMPRESSOR
- K901831 — PRECISION MEDICAL OXYGEN REGULATOR
- K902970 — PRECISION MEDICAL DISPOSABLE HUMIDIFIER
- K902762 — PM14 SOFT AIR COMPRESSOR
- K902916 — PRECISION MEDICAL NEB BLOCK
- K902917 — PRECISION MEDICAL ELIMINATOR
- K854067 — SELECT FLOWMETER
- K850559 — PRESSURE RELIEF ADAPTOR
- K850560 — FLOWMETER, BACKPRESSURE COMPENSATED, THORPE TUBE
- K843223 — FLOW CONTROLLER
Data sourced from openFDA. This site is unofficial and independent of the FDA.