American Endoscopy, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Endoscopy, Inc. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
American Endoscopy, Inc. has 19 FDA 510(k) cleared gastroenterology & urology devices. Based in Mchenry, US.
Historical record: 19 cleared submissions from 1982 to 1985.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Endoscopy, Inc.
19 devices
Cleared
Oct 17, 1985
AMERICAN DILATATION SYSTEM
Gastroenterology & Urology
73d
Cleared
Jul 19, 1984
PROXIMA 1 PH MONITOR
Gastroenterology & Urology
121d
Cleared
Apr 25, 1984
ENDO BITE BLOCK
Ear, Nose, Throat
201d
Cleared
Apr 13, 1984
BIOPSY FORCEPS
Gastroenterology & Urology
49d
Cleared
Jan 03, 1984
TAMPONADE BALLOON CUFF
Gastroenterology & Urology
57d
Cleared
Nov 29, 1983
PERCUTANEOUS ENDOSCOPIC GASTROSCOPY
Gastroenterology & Urology
53d
Cleared
Oct 20, 1983
AUTOMATIC ENDOSCOPE
General Hospital
86d
Cleared
Sep 24, 1982
RETRIEVAL BALLOONS
Gastroenterology & Urology
95d
Cleared
Aug 20, 1982
PIGTAIL STENTS
Gastroenterology & Urology
60d
Cleared
Aug 19, 1982
BALL TIP COAGULATING ELECTRODES
General & Plastic Surgery
37d
Cleared
Aug 10, 1982
PIGTAIL NASAL CATHETERS
Gastroenterology & Urology
50d
Cleared
Jul 20, 1982
LAVAGING CATHETERS
Gastroenterology & Urology
7d