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FDA 510(k)

Ceragem Automatic Thermal Massager, Model CGM-MB-1901

K-Number: K202113 · 2021-03-02

Decision Date2021-03-02
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Ceragem Automatic Thermal Massager, Model CGM-MB-1901 is a medical device manufactured by Ceragem Co., Ltd.. It received FDA 510(k) clearance on 2021-03-02 under approval number K202113. The device is classified under product code JFB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Ceragem Automatic Thermal Massager, Model CGM-MB-1901?

Ceragem Automatic Thermal Massager, Model CGM-MB-1901 is a medical device that received FDA 510(k) clearance on 2021-03-02. It is manufactured by Ceragem Co., Ltd.. The 510(k) number is K202113.

When was Ceragem Automatic Thermal Massager, Model CGM-MB-1901 approved by the FDA?

Ceragem Automatic Thermal Massager, Model CGM-MB-1901 received FDA 510(k) clearance on 2021-03-02, under approval number K202113.

What company makes Ceragem Automatic Thermal Massager, Model CGM-MB-1901?

Ceragem Automatic Thermal Massager, Model CGM-MB-1901 is manufactured by Ceragem Co., Ltd..

What is the FDA product code for Ceragem Automatic Thermal Massager, Model CGM-MB-1901?

The FDA product code for Ceragem Automatic Thermal Massager, Model CGM-MB-1901 is JFB.

Other Devices by Ceragem Co., Ltd.

Related Devices (Code: JFB)

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.