National Wire & Stamping, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
National Wire & Stamping, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
National Wire & Stamping, Inc. has 5 FDA 510(k) cleared medical devices. Based in Englewood, US.
Historical record: 5 cleared submissions from 1986 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by National Wire & Stamping, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - National Wire & Stamping, Inc.
5 devices
Cleared
Dec 30, 1994
ELECTROSURGICAL LOOP ELECTRODE
Obstetrics & Gynecology
351d
Cleared
Apr 19, 1994
MIS ELECTROSURGICAL ELECTRODES
General & Plastic Surgery
96d
Cleared
Jun 19, 1986
ELECTROSURGICAL BLADE ELECTRODE (SOLID TYPE)
General & Plastic Surgery
58d
Cleared
Jun 19, 1986
ELECTROSURGICAL NEEDLE ELECTRODE (SOLID TYPE)
General & Plastic Surgery
51d
Cleared
Jun 19, 1986
BALL ELECTRODES
General & Plastic Surgery
51d