CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE— 510(k) K934337

Name: FDA 510(k) clearance K934337
Creator: U.S. Food and Drug Administration
Published: 1993-11-18

Substantially Equivalent

Cuda Products Co.

FDA 510(k) clearance K934337 for CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE, Substantially Equivalent on 1993-11-18. Applicant: Cuda Products Co.. Device class: 2.

Clearance details

Applicant: Cuda Products Co.
Product code: Code FSW
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1993-09-07
Decision date: 1993-11-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

Download summary PDF View on FDA.gov ↗

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