Zomed Intl. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zomed Intl. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Zomed Intl. has 7 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Historical record: 7 cleared submissions from 1995 to 1996. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Zomed Intl. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Zomed Intl.
7 devices
Cleared
Nov 19, 1996
ZOMED PASSIVE TEMPERATURE PROBE
General Hospital
22d
Cleared
Sep 19, 1996
ZOMED MODEL 30-6 MULTIELECTRODE ARRAY PROBE
General & Plastic Surgery
70d
Cleared
Apr 30, 1996
ZOMED 30F ELECTROSURGICAL PROBE
General & Plastic Surgery
70d
Cleared
Apr 30, 1996
MODEL 200C ELECTROSURGICAL PROBE
General & Plastic Surgery
70d
Cleared
Dec 18, 1995
ZOMED MODEL 20 & 30 ELECTROSURGICAL PROBES
General & Plastic Surgery
49d
Cleared
Oct 04, 1995
ZOMED MODEL 500 ELECTROSURGICAL GENERATOR MODEL 200 ELECTROSURGICAL PROBE
General & Plastic Surgery
155d
Cleared
Jun 19, 1995
ZOMED MODEL 10 CAUTERY BIOPSY DEVICE
General & Plastic Surgery
70d