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

KNIFE MAKER

K Number: K863616 · Decision Sep 25, 1986
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
4
Applicant Total
30
Review Days
9

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Basic Information

Device Name
KNIFE MAKER
K Number
K863616
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 16, 1986
Decision Date
September 25, 1986
Product Code
IDL
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
IDL Microtome, Accessories

Similar 510(k) Clearances

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

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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
K863549 REUSABLE/DISPOSABLE AUTOPSY KNIFE SET
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. →