E & M Engineering, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
E & M Engineering, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
E & M Engineering, Inc. has 6 FDA 510(k) cleared medical devices. Based in Richmond, US.
Historical record: 6 cleared submissions from 1993 to 1999. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by E & M Engineering, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - E & M Engineering, Inc.
6 devices
Cleared
Feb 10, 1999
DISPOSABLE ELECTROSURGERY GROUNDING PAD
General & Plastic Surgery
72d
Cleared
Jul 31, 1996
LOOP/SQUARE ELECTRODE
Obstetrics & Gynecology
457d
Cleared
Feb 10, 1995
BLADE ELECTRODE
General & Plastic Surgery
88d
Cleared
Jun 13, 1994
ELECTROSURGICAL PENCIL
General & Plastic Surgery
175d
Cleared
Jun 06, 1994
REUSABLE, HAND CONTROLLED ESP
General & Plastic Surgery
168d
Cleared
Jul 02, 1993
ELECTROSURGICAL UNIT
General & Plastic Surgery
472d