FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

TISSUE SECTION ADHESIVE

K Number: K881659 · Decision Apr 21, 1988
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
0
Applicant Total
30
Review Days
6

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Basic Information

Device Name
TISSUE SECTION ADHESIVE
K Number
K881659
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.4010
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Surgipath Medical Industries, Inc.
Date Received
April 15, 1988
Decision Date
April 21, 1988
Product Code
IFZ
Advisory Committee
Pathology
Review Advisory Committee
PA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IFZ Gelatin For Specimen Adhesion

Other Clearances by Surgipath Medical Industries, Inc.

K Number Device Name
K883217 SCHIFF REAGENT
K881921 C-E BRUSH
K881922 CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVE
K863549 REUSABLE/DISPOSABLE AUTOPSY KNIFE SET
K863616 KNIFE MAKER
K863548 ROTARY MICROTOME
K863483 CASSETTE EMBOSSEER
K863145 CERVICAL SCRAPERS
K861270 BLUE RIBBON PARAFFIN INFILTRATION/EMBEDDING MED.
K861201 FORMALDEHYDE SOLUTION, 37%
Search all 30 clearances from Surgipath Medical Industries, Inc. →