FDA 510(k), K931464, BAXTER CORONARY ANGIOSCOPE INFLATION DEVICE

510(K) Number: K931464
Device Name: BAXTER CORONARY ANGIOSCOPE INFLATION DEVICE
Manufacturer: BAXTER HEALTHCARE CORP.
Device Classification Name: Angioscope
Regulation Number: 876.1500
Classification Product Code: LYK
Date Received: 03/24/1993
Decision Date: 10/18/1993
Regulation Medical Specialty: Gastroenterology/Urology

77 pages (8 or 65 pages are fully redacted)