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

REUSABLE/DISPOSABLE AUTOPSY KNIFE SET

K Number: K863549 · Decision Sep 30, 1986
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
20
Applicant Total
30
Review Days
18

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Basic Information

Device Name
REUSABLE/DISPOSABLE AUTOPSY KNIFE SET
K Number
K863549
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Surgipath Medical Industries, Inc.
Date Received
September 12, 1986
Decision Date
September 30, 1986
Product Code
EMF
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
EMF Knife, Surgical

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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
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. →