D-Laser Blue, D-Laser 16
K-Number: K210367 · 2022-03-10
Device Summary
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. The listed applicant is Guilin Woodpecker Medical Instrument Co., Ltd.. The 510(k) number is K210367.
When did D-Laser Blue, D-Laser 16 receive FDA 510(k) clearance?
D-Laser Blue, D-Laser 16 received FDA 510(k) clearance on 2022-03-10, under 510(k) number K210367.
Who is the listed applicant for D-Laser Blue, D-Laser 16?
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 D-Laser Blue, D-Laser 16?
The FDA product code for D-Laser Blue, D-Laser 16 is NVK.
Other records listing Guilin Woodpecker Medical Instrument Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: NVK)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.