FDA 510(k), K171899, Revitalair 430F

510(K) Number: K171899
Device Name: Revitalair 430F
Manufacturer: Oxavita S.R.L.
Device Classification Name: Chamber, Hyperbaric
Regulation Number: 868.5470
Classification Product Code: CBF
Date Received: 06/26/2017
Decision Date: 11/22/2019
Regulation Medical Specialty: Anesthesiology

293 pages (1,398 or 1,691 original pages are fully redacted)