Medical Device Manufacturer · US , Mchenry , IL

Surgipath Medical Industries, Inc. - FDA 510(k) Cleared Devices

30 submissions · 30 cleared · Since 1977

Total

Cleared

Denied

Surgipath Medical Industries, Inc. has 30 FDA 510(k) cleared pathology devices. Based in Mchenry, US.

Historical record: 30 cleared submissions from 1977 to 1988.

Browse the complete list of FDA 510(k) cleared pathology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Surgipath Medical Industries, Inc.

30 devices

1-12 of 30

Obstetrics & Gynecology · 71d

Cleared May 25, 1988

CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVE

K881922 · LDZ

Pathology · 16d

Cleared Apr 21, 1988

TISSUE SECTION ADHESIVE

K881659 · IFZ

Pathology · 6d

Cleared Sep 30, 1986

REUSABLE/DISPOSABLE AUTOPSY KNIFE SET

K863549 · EMF

General & Plastic Surgery · 18d

Obstetrics & Gynecology · 4d

Cleared Apr 11, 1986

FORMALDEHYDE SOLUTION, 37%

K861201 · IGG

Pathology · 11d

Cleared Apr 11, 1986

BLUE RIBBON PARAFFIN INFILTRATION/EMBEDDING MED.

K861270 · KEO

Pathology · 7d

Cleared Jan 07, 1986

CLEARENE, CLEARING AGENT

K855109 · KEM

Pathology · 15d

Surgipath Medical Industries, Inc. - FDA 510(k) Cleared Devices

Filters