Surgipath Medical Industries, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgipath Medical Industries, Inc. - FDA 510(k) Cleared Devices
30
Total
30
Cleared
0
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
Cleared
Aug 05, 1988
SCHIFF REAGENT
Pathology
7d
Cleared
Jul 19, 1988
C-E BRUSH
Obstetrics & Gynecology
71d
Cleared
May 25, 1988
CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVE
Pathology
16d
Cleared
Apr 21, 1988
TISSUE SECTION ADHESIVE
Pathology
6d
Cleared
Sep 30, 1986
REUSABLE/DISPOSABLE AUTOPSY KNIFE SET
General & Plastic Surgery
18d
Cleared
Sep 25, 1986
KNIFE MAKER
Pathology
9d
Cleared
Sep 19, 1986
ROTARY MICROTOME
Pathology
7d
Cleared
Sep 16, 1986
CASSETTE EMBOSSEER
Pathology
7d
Cleared
Aug 19, 1986
CERVICAL SCRAPERS
Obstetrics & Gynecology
4d
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