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FDA 510(k)

Irradiation Aesthetic Device

K-Number: K171835 · 2018-01-30

ApplicantChongqing Peninsula Medical Technology Co., Ltd.
Decision Date2018-01-30
Product CodeOAP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Irradiation Aesthetic Device is a medical device manufactured by Chongqing Peninsula Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2018-01-30 under approval number K171835. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Irradiation Aesthetic Device?

Irradiation Aesthetic Device is a medical device that received FDA 510(k) clearance on 2018-01-30. It is manufactured by Chongqing Peninsula Medical Technology Co., Ltd.. The 510(k) number is K171835.

When was Irradiation Aesthetic Device approved by the FDA?

Irradiation Aesthetic Device received FDA 510(k) clearance on 2018-01-30, under approval number K171835.

What company makes Irradiation Aesthetic Device?

Irradiation Aesthetic Device is manufactured by Chongqing Peninsula Medical Technology Co., Ltd..

What is the FDA product code for Irradiation Aesthetic Device?

The FDA product code for Irradiation Aesthetic Device is OAP.

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Other Devices by Chongqing Peninsula Medical Technology Co., Ltd.

K172273308nm Excimer System K192642308nm Excimer System K192552Irradiation Cosmetic Device

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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.

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