PROXENON 350, MODEL 902XX— 510(k) K071218

Substantially Equivalent

Welch Allyn, Inc.

FDA 510(k) clearance K071218 for PROXENON 350, MODEL 902XX, Substantially Equivalent on 2007-06-14. Applicant: Welch Allyn, Inc.. Device class: 2.

Clearance details

Applicant: Welch Allyn, Inc.
Product code: Code FST
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 2007-05-02
Decision date: 2007-06-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Skaneateles Falls, NY, US

Download summary PDF View on FDA.gov ↗

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