FDA 510(k) Application Details - K990927

Device Classification Name	Chamber, Hyperbaric   More FDA Info for this Device
510(K) Number	K990927
Device Name	Chamber, Hyperbaric
Applicant	PERRY BAROMEDICAL CORP. 3660 INTERSTATE PKWY. RIVERA BEACH, FL 33404 US Other 510(k) Applications for this Company
Contact	JAMES P DODSON 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	03/19/1999
Decision Date	11/12/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review