FDA 510(k), K874752, GAMOW HYPERBARIC BAG
FDA 510(k), K874752, GAMOW HYPERBARIC BAG
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510(K) Number: K874752
Device Name: GAMOW HYPERBARIC BAG
Manufacturer: HYPERBARIC AEROBICS, LTD.
Device Classification Name: Chamber, Hyperbaric
Regulation Number: 868.5470
Classification Product Code: CBF
Date Received: 11/18/1987
Decision Date: 02/02/1988
Regulation Medical Specialty: Anesthesiology
Device Name: GAMOW HYPERBARIC BAG
Manufacturer: HYPERBARIC AEROBICS, LTD.
Device Classification Name: Chamber, Hyperbaric
Regulation Number: 868.5470
Classification Product Code: CBF
Date Received: 11/18/1987
Decision Date: 02/02/1988
Regulation Medical Specialty: Anesthesiology
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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