Medical Device Manufacturer · US , Rockville , MD

Jomed, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2001

Recent clearances: JOVUS EAGLE EYE F/X 2.9F IVUS CATHETER, MODEL 85900, IN-VISION IMAGING SYSTEM, JOWIRE ASAHI PTCA CATHETER GUIDE WIRES, MODELS AG145300,141300,142300,132200,14M350,14M345,14M360,143390,141002

View 6 510(k) Devices ↓

6

Total

6

Cleared

0

Denied

Jomed, Inc. has 6 FDA 510(k) cleared medical devices. Based in Rockville, US.

Historical record: 6 cleared submissions from 2001 to 2003. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Jomed, Inc. Filter by specialty or product code using the sidebar.

Jomed, Inc. is one of 25817 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Jomed, Inc.

6 devices

1-6 of 6

Cleared Jun 23, 2003

JOVUS EAGLE EYE F/X 2.9F IVUS CATHETER, MODEL 85900

Cardiovascular · 55d

Cleared May 28, 2003

IN-VISION IMAGING SYSTEM

Cardiovascular · 48d

Cleared May 14, 2003

JOWIRE ASAHI PTCA CATHETER GUIDE WIRES, MODELS...

Cardiovascular · 22d

Cleared Dec 16, 2002

JOWIRE NEO'S PTCA CATHETER GUIDEWIRES, MODELS AG141000, AG142000, AG143000,...

Cardiovascular · 118d

Cleared May 17, 2002

SMARTWIRE/SMARTMAP PRESSURE SYSTEM

Cardiovascular · 30d

Cleared Jan 18, 2001

Cardiovascular · 29d