BR-2 BIOREST— 510(k) K873920

Name: FDA 510(k) clearance K873920
Creator: U.S. Food and Drug Administration
Published: 1987-12-29

Substantially Equivalent for Some Indications

Biorest, Inc.

FDA 510(k) clearance K873920 for BR-2 BIOREST, Substantially Equivalent for Some Indications on 1987-12-29. Applicant: Biorest, Inc.. Device class: 2.

Clearance details

Applicant: Biorest, Inc.
Product code: Code QJQ
Device class: Class 2
Regulation: 21 CFR 882.5800
Advisory panel: Neurology
Date received: 1987-09-25
Decision date: 1987-12-29
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: San Antonio, TX, US

Download summary PDF View on FDA.gov ↗

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