FDA 510(k) Application Details - K963349

Device Classification Name	Compressor, Air, Portable   More FDA Info for this Device
510(K) Number	K963349
Device Name	Compressor, Air, Portable
Applicant	DEVILBISS HEALTH CARE, INC. 1200 EAST MAIN ST. P.O.BOX 635 SOMERSET, PA 15501-0635 US Other 510(k) Applications for this Company
Contact	MATT SMITH Other 510(k) Applications for this Contact
Regulation Number	868.6250   More FDA Info for this Regulation Number
Classification Product Code	BTI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/26/1996
Decision Date	06/13/1997
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