KNIFE MAKER— 510(k) K863616

Substantially Equivalent

Surgipath Medical Industries, Inc.

FDA 510(k) clearance K863616 for KNIFE MAKER, Substantially Equivalent on 1986-09-25. Applicant: Surgipath Medical Industries, Inc.. Device class: 1.

Clearance details

Applicant: Surgipath Medical Industries, Inc.
Product code: Code IDL
Device class: Class 1
Regulation: 21 CFR 864.3010
Advisory panel: Pathology
Date received: 1986-09-16
Decision date: 1986-09-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grayslake, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IDL

K831921 — DISPOSABLE MICROTOME BLADES1983-07-29
K831308 — DISPOSABLE MICROTOME BLADE1983-05-16
K813430 — TISSUE PROCESSING CASSETTES & ACCESS1981-12-29
K801426 — TISSUE-TEK III MICROJECT DISP. BLADE SYS1980-07-28

More clearances from Surgipath Medical Industries, Inc.

K883217 — SCHIFF REAGENT1988-08-05
K881921 — C-E BRUSH1988-07-19
K881922 — CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVE1988-05-25
K881659 — TISSUE SECTION ADHESIVE1988-04-21
K863549 — REUSABLE/DISPOSABLE AUTOPSY KNIFE SET1986-09-30

Data sourced from openFDA. This site is unofficial and independent of the FDA.