Intl. Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intl. Medical, Inc. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Intl. Medical, Inc. has 17 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 17 cleared submissions from 1979 to 1997.
Browse the FDA 510(k) cleared devices submitted by Intl. Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Intl. Medical, Inc.
17 devices
Cleared
Jun 13, 1997
PEAK FLOW METER
Anesthesiology
123d
Cleared
Nov 14, 1994
HOT BIOPSY FORCEPS
Gastroenterology & Urology
139d
Cleared
Aug 17, 1994
AMERICAN CATHETER E.R.C.P. CANNULA
Gastroenterology & Urology
203d
Cleared
Jul 21, 1994
AMERICAN CATHETER POLY-SNARE
Gastroenterology & Urology
177d
Cleared
Jun 24, 1994
AMERICAN CATHETER SPHINCTEROTOME
Gastroenterology & Urology
56d
Cleared
Sep 03, 1993
DURHAM
General Hospital
220d
Cleared
Sep 03, 1993
DURHAM
General Hospital
220d
Cleared
Dec 07, 1992
AMCATH DISPOSABLE CYTOLOGY BRUSH
Gastroenterology & Urology
160d
Cleared
Jan 10, 1992
AMCATH DISPOSABLE BIOPSY FORCEPS
Gastroenterology & Urology
57d
Cleared
Sep 19, 1991
AMCATH DISPOSABLE TROCAR AND TROCAR SLEEVE
General & Plastic Surgery
78d
Cleared
Jul 11, 1991
AMCATH DISPOSABLE MICRO SCISSORS
General & Plastic Surgery
29d
Cleared
Jun 20, 1990
AMCATH COAGULATION PROBE
Obstetrics & Gynecology
12d