FORMALIN BUFFER CONCENTRATE— 510(k) K771201

Name: FDA 510(k) clearance K771201
Creator: U.S. Food and Drug Administration
Published: 1977-08-22

Substantially Equivalent

Central Labs. Assoc. MD Pathologists

FDA 510(k) clearance K771201 for FORMALIN BUFFER CONCENTRATE, Substantially Equivalent on 1977-08-22. Applicant: Central Labs. Assoc. MD Pathologists. Device class: 1.

Clearance details

Applicant: Central Labs. Assoc. MD Pathologists
Product code: Code IGG
Device class: Class 1
Regulation: 21 CFR 864.4010
Advisory panel: Pathology
Date received: 1977-07-05
Decision date: 1977-08-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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