Airsep Corp.
Airsep Corp. holds FDA 510(k) medical device clearances, first cleared 1987, most recent 2011.
Top product codes for Airsep Corp.
Recent clearances by Airsep Corp.
- K101154 — CENTROX, RELIANT, ULTROX, AS-D+, AS-E, AS-G, AS-J, AS-K AND AS-L
- K080348 — OXISCAN II DATA MANAGEMENT SYSTEM
- K020324 — LIFESTYLE OXYGEN CONCENTRATOR
- K012037 — HEALTHLIFE OXYGEN CONCENTRATOR MODEL AS009
- K000963 — DA VINCHI EEG AND EMG/EP SYSTEMS
- K001579 — IMPULSE SELECT
- K001467 — DA VINCHI EMG/EP ISA1004EP
- K001013 — MONET ACQUISITION SYSTEM FOR EEG AND POLYSOMNOGRAPHY
- K992283 — ARTISAN ACQUISITION SYSTEM FOR EEG AND POLYSOMNOGRAPHY
- K983002 — MYSTIQUE ULTRASONIC NEBULIZER
- K960309 — AIRSEP NEWLIFE DUAL SIX OXYGEN CONCENTRATOR (MODIFICATION)
- K962865 — REMBRANDT SYSTEM
- K962766 — AIRSEP IMPULSE
- K943207 — NITELIFE BI-LEVEL CPAP
- K951882 — ECO CHECK (ECOVALVE AND OXYGEN MONITOR)
- K944020 — AIRSEP NEWLIFE AIR OUTLET OPTION
- K884581 — RELIANT OXYGEN CONCENTRATOR
- K872534 — 4LYF OXYGEN CONCENTRATOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.