Dermatological diode laser system
K-Number: K212478 · 2022-01-14
Device Summary
Frequently Asked Questions
What is the Dermatological diode laser system?
Dermatological diode laser system is a medical device that received FDA 510(k) clearance on 2022-01-14. The listed applicant is Beijing Stelle Laser Technology Co., Ltd.. The 510(k) number is K212478.
When did Dermatological diode laser system receive FDA 510(k) clearance?
Dermatological diode laser system received FDA 510(k) clearance on 2022-01-14, under 510(k) number K212478.
Who is the listed applicant for Dermatological diode laser system?
The FDA 510(k) record lists Beijing Stelle Laser Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dermatological diode laser system?
The FDA product code for Dermatological diode laser system is GEX. This falls under the Gastroenterology category.
Related Devices (Code: GEX)
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
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