PROTRON TECHNOLOGIES, LLC STETHOTRON— 510(k) K082771

Name: FDA 510(k) clearance K082771
Creator: U.S. Food and Drug Administration
Published: 2009-02-27

Substantially Equivalent

Protron Technologies, LLC

FDA 510(k) clearance K082771 for PROTRON TECHNOLOGIES, LLC STETHOTRON, Substantially Equivalent on 2009-02-27. Applicant: Protron Technologies, LLC. Device class: 2.

Clearance details

Applicant: Protron Technologies, LLC
Product code: Code DQD
Device class: Class 2
Regulation: 21 CFR 870.1875
Advisory panel: Cardiovascular
Date received: 2008-09-22
Decision date: 2009-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Leonia, NJ, US

Download summary PDF View on FDA.gov ↗

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