Medical Device Manufacturer · DE , Germany

Mahe-Medizintechnik - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1993

8

Total

8

Cleared

0

Denied

Mahe-Medizintechnik has 8 FDA 510(k) cleared medical devices. Based in Germany, DE.

Historical record: 8 cleared submissions from 1993 to 1994. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Mahe-Medizintechnik Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Mahe-Medizintechnik

8 devices

1-8 of 8

Cleared Nov 02, 1994

MAHE INSTRUMENTS

General & Plastic Surgery · 141d

Cleared Aug 23, 1994

TROCAR WITH SHIELD

General & Plastic Surgery · 70d

Cleared Jun 27, 1994

COAGULATOR, LAPAROSCOPIC, LUNIPOLAR/ACCESSORIES

Obstetrics & Gynecology · 333d

Cleared May 26, 1994

FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSY

Obstetrics & Gynecology · 301d

Cleared Mar 23, 1994

FORCEPS, ENT INSTR, ENT MANUAL SURG RETRACT/ALL TYPE

Ear, Nose, Throat · 237d

Cleared Mar 14, 1994

MAHE INSTRUMENTS

General & Plastic Surgery · 122d

Cleared Feb 01, 1994

Orthopedic · 187d

Cleared Jul 22, 1993

MICROSURGICAL INSTRUMENTS

General & Plastic Surgery · 258d