FDA 510(k) Application Details - K971670

Device Classification Name	Recorder, Magnetic Tape, Medical   More FDA Info for this Device
510(K) Number	K971670
Device Name	Recorder, Magnetic Tape, Medical
Applicant	GALIX BIOMEDICAL INSTRUMENTATION, INC. 2555 COLLINS AVE., C-5 MIAMI BEACH, FL 33140 US Other 510(k) Applications for this Company
Contact	JORDAN GAVRIELIDES Other 510(k) Applications for this Contact
Regulation Number	870.2800   More FDA Info for this Regulation Number
Classification Product Code	DSH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/06/1997
Decision Date	01/29/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review