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FDA 510(k)

LED.L, LED.M, LED.G, LED.B

K-Number: K080025 · 2008-03-19

ApplicantGuilin Woodpecker Medical Instrument Co., Ltd.
Decision Date2008-03-19
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LED.L, LED.M, LED.G, LED.B is the device name listed in this FDA 510(k) record. The listed applicant is Guilin Woodpecker Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2008-03-19 under 510(k) number K080025. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LED.L, LED.M, LED.G, LED.B?

LED.L, LED.M, LED.G, LED.B is a medical device that received FDA 510(k) clearance on 2008-03-19. The listed applicant is Guilin Woodpecker Medical Instrument Co., Ltd.. The 510(k) number is K080025.

When did LED.L, LED.M, LED.G, LED.B receive FDA 510(k) clearance?

LED.L, LED.M, LED.G, LED.B received FDA 510(k) clearance on 2008-03-19, under 510(k) number K080025.

Who is the listed applicant for LED.L, LED.M, LED.G, LED.B?

The FDA 510(k) record lists Guilin Woodpecker Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LED.L, LED.M, LED.G, LED.B?

The FDA product code for LED.L, LED.M, LED.G, LED.B is EBZ.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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