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FDA 510(k), K862198, SIGMA II - DUAL PLACE HYPERBARIC CHAMBER
FDA 510(k), K862198, SIGMA II - DUAL PLACE HYPERBARIC CHAMBER
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510(K) Number: K862198
Device Name: SIGMA II - DUAL PLACE HYPERBARIC CHAMBER
Manufacturer: PERRY BAROMEDICAL SERVICES
Device Classification Name: chamber, hyperbaric
Regulation Number: 868.5470
Classification Product Code: CBF
Date Received: 06/09/1986
Decision Date: 11/12/1986
Regulation Medical Specialty: Anesthesiology
Device Name: SIGMA II - DUAL PLACE HYPERBARIC CHAMBER
Manufacturer: PERRY BAROMEDICAL SERVICES
Device Classification Name: chamber, hyperbaric
Regulation Number: 868.5470
Classification Product Code: CBF
Date Received: 06/09/1986
Decision Date: 11/12/1986
Regulation Medical Specialty: Anesthesiology
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- 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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