BRAY RONGEUR— 510(k) K954699

Name: FDA 510(k) clearance K954699
Creator: U.S. Food and Drug Administration
Published: 1995-12-06

Substantially Equivalent

Johnson & Johnson Professionals, Inc.

FDA 510(k) clearance K954699 for BRAY RONGEUR, Substantially Equivalent on 1995-12-06. Applicant: Johnson & Johnson Professionals, Inc.. Device class: 2.

Clearance details

Applicant: Johnson & Johnson Professionals, Inc.
Product code: Code HAE
Device class: Class 2
Regulation: 21 CFR 882.4840
Advisory panel: Neurology
Date received: 1995-10-12
Decision date: 1995-12-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raritan, NJ, US

Download summary PDF View on FDA.gov ↗

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