FDA 510(k) Application Details - K971129

Device Classification Name	Generator, Oxygen, Portable   More FDA Info for this Device
510(K) Number	K971129
Device Name	Generator, Oxygen, Portable
Applicant	ARBOR RESEARCH CORP. 806 AIRPORT BLVD. ANN ARBOR, MI 48108 US Other 510(k) Applications for this Company
Contact	BLAKE M PATERSON Other 510(k) Applications for this Contact
Regulation Number	868.5440   More FDA Info for this Regulation Number
Classification Product Code	CAW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/27/1997
Decision Date	06/24/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review