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FDA 510(k), K220290, Revitalair 430+
FDA 510(k), K220290, Revitalair 430+
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$737.80 USD
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$737.80 USD
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510(K) Number: K220290
Device Name: Revitalair 430+
Manufacturer: US Hyperbaric Network
Device Classification Name: Chamber, Hyperbaric
Regulation Number: 868.5470
Classification Product Code: CBF
Date Received: 02/01/2022
Decision Date: 05/04/2023
Regulation Medical Specialty: Anesthesiology
Total Pages: 2,537
Fully Redacted Pages: 2,200
Content Pages: 337
Device Name: Revitalair 430+
Manufacturer: US Hyperbaric Network
Device Classification Name: Chamber, Hyperbaric
Regulation Number: 868.5470
Classification Product Code: CBF
Date Received: 02/01/2022
Decision Date: 05/04/2023
Regulation Medical Specialty: Anesthesiology
Total Pages: 2,537
Fully Redacted Pages: 2,200
Content Pages: 337
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