Medical Device Manufacturer · US , Mchenry , IL

Med General - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1977

12

Total

12

Cleared

0

Denied

Med General has 12 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 12 cleared submissions from 1977 to 1979.

Browse the FDA 510(k) cleared devices submitted by Med General Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Med General

12 devices

1-12 of 12

Cleared Aug 03, 1979

CEPTORTRODE WITH CEPTOR HESIVE

Neurology · 52d

Cleared Jun 22, 1979

SINGLE-USE MINI-BULLDOG

Cardiovascular · 10d

Cleared Apr 23, 1979

General & Plastic Surgery · 5d

Cleared Feb 26, 1979

Neurology · 21d

Cleared Dec 15, 1978

MEDGENERAL SINGLE-USE BULLDOG

General & Plastic Surgery · 14d

Cleared Nov 03, 1978

Physical Medicine · 106d

Cleared Aug 14, 1978

Physical Medicine · 119d

Cleared May 12, 1978

STIMULATORS, NERVE, ELECTRICAL

Neurology · 16d

Cleared Feb 03, 1978

Cardiovascular · 11d

Cleared Dec 13, 1977

General & Plastic Surgery · 96d

Cleared Dec 13, 1977

VESSEL-STABILIZER

General & Plastic Surgery · 96d

Cleared Sep 30, 1977

Anesthesiology · 11d