Thermedics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Thermedics, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Thermedics, Inc. has 4 FDA 510(k) cleared medical devices. Based in Woburn, US.
Historical record: 4 cleared submissions from 1985 to 1989. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Thermedics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Thermedics, Inc.
4 devices
Cleared
Sep 26, 1989
DERMAPORT VASCULAR ACCESS DEVICE MODEL NO. 50-1000
Cardiovascular
105d
Cleared
Sep 09, 1986
PERITONEAL DIALYSIS CATHETERS
Gastroenterology & Urology
25d
Cleared
Jan 09, 1986
ACUTE PERITONEAL DIALYSIS CATHETERS
Gastroenterology & Urology
29d
Cleared
Apr 15, 1985
WOUND DRESSING MODEL ZB-6
General & Plastic Surgery
96d