Intense pulsed light device, Model(s): DE01A-B, DE01A-G, DE01B-B, DE01B-G, DE01C-B, DE01C-G, DE02A-B, DE02A-G, DE02B-B, DE02B-G, DE02C-B, DE02C-G.— 510(k) K231613

Substantially Equivalent

Zhuzhou Goldenhot Medical Technology Co., Ltd.

FDA 510(k) clearance K231613 for Intense pulsed light device, Model(s): DE01A-B, DE01A-G, DE01B-B, DE01B-G, DE01C-B, DE01C-G, DE02A-B, DE02A-G, DE02B-B, DE02B-G, DE02C-B, DE02C-G., Substantially Equivalent on 2023-07-31. Applicant: Zhuzhou Goldenhot Medical Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant
Zhuzhou Goldenhot Medical Technology Co., Ltd.
Product code
Code OHT
Device class
Class 2
Regulation
21 CFR 878.4810
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Zhuzhou, CN
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