LED.L, LED.M, LED.G, LED.B— 510(k) K080025

Name: FDA 510(k) clearance K080025
Creator: U.S. Food and Drug Administration
Published: 2008-03-19

Substantially Equivalent

Guilin Woodpecker Medical Instrument Co., Ltd.

FDA 510(k) clearance K080025 for LED.L, LED.M, LED.G, LED.B, Substantially Equivalent on 2008-03-19. Applicant: Guilin Woodpecker Medical Instrument Co., Ltd.. Device class: 2.

Clearance details

Applicant: Guilin Woodpecker Medical Instrument Co., Ltd.
Product code: Code EBZ
Device class: Class 2
Regulation: 21 CFR 872.6070
Advisory panel: Dental
Date received: 2008-01-04
Decision date: 2008-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Flintville, TN, US

Download summary PDF View on FDA.gov ↗

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