ACRYTOL, MOUNTING MEDIUM— 510(k) K810323

Substantially Equivalent

Surgipath

FDA 510(k) clearance K810323 for ACRYTOL, MOUNTING MEDIUM, Substantially Equivalent on 1981-03-06. Applicant: Surgipath. Device class: 1.

Clearance details

Applicant: Surgipath
Product code: Code KEP
Device class: Class 1
Regulation: 21 CFR 864.4010
Advisory panel: Pathology
Date received: 1981-02-06
Decision date: 1981-03-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Recent devices under product code KEP

K830659 — CLEARIUM, MOUNTING MEDIUM1983-03-17
K800847 — ENTELLAN1980-05-08

More clearances from Surgipath

K820027 — MODIFIED EA 501982-02-04
K812940 — 10% NEUTRAL BUFFERED FORMALIN CONCENT1981-12-10
K812086 — EA 651981-08-13
K812087 — EA 501981-08-13
K811825 — ORANGE G-61981-07-10

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