C-E BRUSH— 510(k) K881921

Substantially Equivalent

Surgipath Medical Industries, Inc.

FDA 510(k) clearance K881921 for C-E BRUSH, Substantially Equivalent on 1988-07-19. Applicant: Surgipath Medical Industries, Inc.. Device class: 2.

Clearance details

Applicant: Surgipath Medical Industries, Inc.
Product code: Code HHT
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1988-05-09
Decision date: 1988-07-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grayslake, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Surgipath Medical Industries, Inc.

K883217 — SCHIFF REAGENT1988-08-05
K881922 — CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVE1988-05-25
K881659 — TISSUE SECTION ADHESIVE1988-04-21
K863549 — REUSABLE/DISPOSABLE AUTOPSY KNIFE SET1986-09-30
K863616 — KNIFE MAKER1986-09-25

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