D-Laser Blue, D-Laser 16
K-Number: K210367 · 2022-03-10
Decision Date2022-03-10
Product CodeNVK
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
D-Laser Blue, D-Laser 16 is a medical device manufactured by Guilin Woodpecker Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2022-03-10 under approval number K210367. The device is classified under product code NVK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the D-Laser Blue, D-Laser 16?
D-Laser Blue, D-Laser 16 is a medical device that received FDA 510(k) clearance on 2022-03-10. It is manufactured by Guilin Woodpecker Medical Instrument Co., Ltd.. The 510(k) number is K210367.
When was D-Laser Blue, D-Laser 16 approved by the FDA?
D-Laser Blue, D-Laser 16 received FDA 510(k) clearance on 2022-03-10, under approval number K210367.
What company makes D-Laser Blue, D-Laser 16?
D-Laser Blue, D-Laser 16 is manufactured by Guilin Woodpecker Medical Instrument Co., Ltd..
What is the FDA product code for D-Laser Blue, D-Laser 16?
The FDA product code for D-Laser Blue, D-Laser 16 is NVK.
Other Devices by Guilin Woodpecker Medical Instrument Co., Ltd.
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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.