Medical Device Manufacturer · US , Fredericktown , OH

M & R Mfg., Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1996

Total

Cleared

Denied

M & R Mfg., Inc. has 2 FDA 510(k) cleared medical devices. Based in Fredericktown, US.

Historical record: 2 cleared submissions from 1996 to 1997. Primary specialty: Neurology.

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

M & R Mfg., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - M & R Mfg., Inc.

2 devices

1-2 of 2