SATURN LIGHT— 510(k) K935102

Substantially Equivalent

Burton Medical Products Corp.

FDA 510(k) clearance K935102 for SATURN LIGHT, Substantially Equivalent on 1994-06-27. Applicant: Burton Medical Products Corp.. Device class: 2.

Clearance details

Applicant: Burton Medical Products Corp.
Product code: Code FTA
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1993-10-22
Decision date: 1994-06-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Van Nuys, CA, 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.