Medical Device Manufacturer · US , Mchenry , IL

Medi-Spec - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1978

8

Total

8

Cleared

0

Denied

Medi-Spec has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 8 cleared submissions from 1978 to 1984.

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

Medi-Spec 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 - Medi-Spec

8 devices

1-8 of 8

Cleared Feb 04, 1984

LAMINARIA JAPONICA CERVICAL DILATOR

Obstetrics & Gynecology · 149d

Cleared Oct 26, 1981

General & Plastic Surgery · 34d

Cleared Oct 08, 1981

UTERINE ASPIRATION CURETTES(RIGID&FLEX)

Obstetrics & Gynecology · 44d

Cleared Aug 04, 1980

STERILE CAST PADDING

Ophthalmic · 27d

Cleared Apr 24, 1980

MEDSPEC OPERATIVE OPTHALMIC KIT

General & Plastic Surgery · 58d

Cleared Mar 12, 1980

STERILE DRESSING PACK

General Hospital · 8d

Cleared Jun 05, 1979

General & Plastic Surgery · 14d

Cleared Aug 21, 1978

General Hospital · 138d