Imagyn Medical Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Imagyn Medical Technologies, Inc. - FDA 510(k) Cleared Devices
7
Total
6
Cleared
0
Denied
Imagyn Medical Technologies, Inc. has 6 FDA 510(k) cleared medical devices. Based in Richland, US.
Historical record: 6 cleared submissions from 1998 to 2003.
Browse the FDA 510(k) cleared devices submitted by Imagyn Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Imagyn Medical Technologies, Inc.
7 devices
Cleared
Sep 04, 2003
ECOM CV4 ENDOTRACHEAL CARDIAC OUTPUT MONITOR
Cardiovascular
23d
Cleared
Mar 07, 2003
IM2001 PULSE OXIMETER
Anesthesiology
570d
Cleared
Dec 03, 2001
IMAGYN ISOSLEEVE / ISOSTAR NEEDLE SYSTEM
Radiology
319d
Cleared
Jun 17, 1999
ISOSTAR I-125 INTERSTITIAL SEED, MODEL IS-12501
Radiology
45d
Cleared
May 01, 1998
OAC (OPTICAL ASPIRATING CURETTE)
Obstetrics & Gynecology
112d
Cleared
Mar 11, 1998
IMPOWER EXTERNAL VACUUM SYSTEM
Gastroenterology & Urology
44d
Cleared
Feb 25, 1998
ERECAID SYSTEM/STAY EREC SYSTEM
Gastroenterology & Urology
112d