AIRSEP NEWLIFE DUAL SIX OXYGEN CONCENTRATOR (MODIFICATION) — Airsep Corp. (510(k) K960309)
AIRSEP NEWLIFE DUAL SIX OXYGEN CONCENTRATOR (MODIFICATION) — Airsep Corp. (510(k) K960309) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: AIRSEP NEWLIFE DUAL SIX OXYGEN CONCENTRATOR (MODIFICATION); Applicant: Airsep Corp.; Clearance track: 510(k).
| Device name | AIRSEP NEWLIFE DUAL SIX OXYGEN CONCENTRATOR (MODIFICATION) |
|---|---|
| Applicant | Airsep Corp. |
| Clearance track | 510(k) |
| Submission number | K960309 |
| Decision | Substantially Equivalent |
| Decision date | 1997-02-28 |
| Date received | 1996-01-05 |
| Product code | CAW |
| Device class | 2 |
| Medical specialty | Anesthesiology |
| Applicant location | NY, US |
| Source | openFDA device |
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