Medical Device Manufacturer · US , Mchenry , IL

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

30 submissions · 30 cleared · Since 1977

30

Total

30

Cleared

0

Denied

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

25 devices

1-12 of 25

Cleared Aug 05, 1988

Pathology · 7d

Cleared May 25, 1988

CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVE

Pathology · 16d

Cleared Apr 21, 1988

TISSUE SECTION ADHESIVE

Pathology · 6d

Cleared Sep 25, 1986

Pathology · 9d

Cleared Sep 19, 1986

ROTARY MICROTOME

Pathology · 7d

Cleared Sep 16, 1986

CASSETTE EMBOSSEER

Pathology · 7d

Cleared Apr 11, 1986

FORMALDEHYDE SOLUTION, 37%

Pathology · 11d

Cleared Apr 11, 1986

BLUE RIBBON PARAFFIN INFILTRATION/EMBEDDING MED.

Pathology · 7d

Cleared Jan 07, 1986

CLEARENE, CLEARING AGENT

Pathology · 15d

Cleared Aug 28, 1985

PREFILLED SPECIMEN JARS 10% NEUTRAL BUF-FORMALIN

Pathology · 8d

Cleared Jun 10, 1985

SED-FIX CONCENTRATE

Pathology · 32d

Cleared Mar 25, 1985

Pathology · 20d