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FDA 510(k)

Intense Pulsed Light System (ST-690)

K-Number: K240482 · 2024-05-17

ApplicantSmedtrum Medical Technology Co., Ltd.
Decision Date2024-05-17
Product CodeONF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Intense Pulsed Light System (ST-690) is a medical device manufactured by Smedtrum Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-05-17 under approval number K240482. 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 System (ST-690)?

Intense Pulsed Light System (ST-690) is a medical device that received FDA 510(k) clearance on 2024-05-17. It is manufactured by Smedtrum Medical Technology Co., Ltd.. The 510(k) number is K240482.

When was Intense Pulsed Light System (ST-690) approved by the FDA?

Intense Pulsed Light System (ST-690) received FDA 510(k) clearance on 2024-05-17, under approval number K240482.

What company makes Intense Pulsed Light System (ST-690)?

Intense Pulsed Light System (ST-690) is manufactured by Smedtrum Medical Technology Co., Ltd..

What is the FDA product code for Intense Pulsed Light System (ST-690)?

The FDA product code for Intense Pulsed Light System (ST-690) is ONF.

Related Clinical Trials

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Other Devices by Smedtrum Medical Technology Co., Ltd.

K221597CO2 Laser System K231394Intense Pulsed Light System K230580Diode Laser System K240118Picosecond Nd:YAG Laser System

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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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