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

CASSETTE EMBOSSEER

K Number: K863483 · Decision Sep 16, 1986
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
4
Applicant Total
30
Review Days
7

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
CASSETTE EMBOSSEER
K Number
K863483
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.3010
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Surgipath Medical Industries, Inc.
Date Received
September 9, 1986
Decision Date
September 16, 1986
Product Code
IDZ
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
IDZ Cassettes, Tissue

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (IDZ), ordered by most recent decision date.

View all

Other Clearances by Surgipath Medical Industries, Inc.

K Number Device Name
K883217 SCHIFF REAGENT
K881921 C-E BRUSH
K881922 CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVE
K881659 TISSUE SECTION ADHESIVE
K863549 REUSABLE/DISPOSABLE AUTOPSY KNIFE SET
K863616 KNIFE MAKER
K863548 ROTARY MICROTOME
K863145 CERVICAL SCRAPERS
K861270 BLUE RIBBON PARAFFIN INFILTRATION/EMBEDDING MED.
K861201 FORMALDEHYDE SOLUTION, 37%
Search all 30 clearances from Surgipath Medical Industries, Inc. →