Laser Therapy Device
K-Number: K202980 · 2020-11-19
Device Summary
Frequently Asked Questions
What is the Laser Therapy Device?
Laser Therapy Device is a medical device that received FDA 510(k) clearance on 2020-11-19. The listed applicant is Shenzhen Leaflife Technology Co., Ltd.. The 510(k) number is K202980.
When did Laser Therapy Device receive FDA 510(k) clearance?
Laser Therapy Device received FDA 510(k) clearance on 2020-11-19, under 510(k) number K202980.
Who is the listed applicant for Laser Therapy Device?
The FDA 510(k) record lists Shenzhen Leaflife Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Laser Therapy Device?
The FDA product code for Laser Therapy Device is GEX. This falls under the Gastroenterology category.
Other records listing Shenzhen Leaflife Technology 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: 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.