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FDA 510(k)

Intense Pulsed Light Equipment

K-Number: K220385 · 2022-08-12

ApplicantBeijing Globalipl Development Co., Ltd.
Decision Date2022-08-12
Product CodeONF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Intense Pulsed Light Equipment is a medical device manufactured by Beijing Globalipl Development Co., Ltd.. It received FDA 510(k) clearance on 2022-08-12 under approval number K220385. The device is classified under product code ONF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Intense Pulsed Light Equipment?

Intense Pulsed Light Equipment is a medical device that received FDA 510(k) clearance on 2022-08-12. It is manufactured by Beijing Globalipl Development Co., Ltd.. The 510(k) number is K220385.

When was Intense Pulsed Light Equipment approved by the FDA?

Intense Pulsed Light Equipment received FDA 510(k) clearance on 2022-08-12, under approval number K220385.

What company makes Intense Pulsed Light Equipment?

Intense Pulsed Light Equipment is manufactured by Beijing Globalipl Development Co., Ltd..

What is the FDA product code for Intense Pulsed Light Equipment?

The FDA product code for Intense Pulsed Light Equipment is ONF.

Related Clinical Trials

NCT07599709 LONG PULSED ND:YAG LASER (1064 NM) VERSUS INTENSE PULSED LIGHT IN TREATMENT OF TRAUMATIC AND POST-SURGICAL ERYTHEMATOUS SCARS COMPLETED NCT06351046 Preventive Interventions for Chronic Pain Worsening RECRUITING NCT06934135 Trial of Transcranial Photobiomodulation for Depression With PET and EEG Outcomes COMPLETED NCT05226637 Does ESWT With BoNTA Treatment Improve Outcomes When Compared to Standard Management for Upper Limb Spasticity Patient. RECRUITING NCT07474883 Efficacy of 0.5% Topical Timolol Eye Drops in the Treatment of Post-Inflammatory Erythema Following Acne Vulgaris RECRUITING

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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