FDA 510(k) Application Details - K072427

Device Classification Name	Chamber, Hyperbaric   More FDA Info for this Device
510(K) Number	K072427
Device Name	Chamber, Hyperbaric
Applicant	PERRY BAROMEDICAL CORP. 3660 INTERSTATE PKWY. RIVIERA BEACH, FL 33404 US Other 510(k) Applications for this Company
Contact	JOHN CROCKER Other 510(k) Applications for this Contact
Regulation Number	868.5470   More FDA Info for this Regulation Number
Classification Product Code	CBF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/29/2007
Decision Date	06/11/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review