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FDA 510(k)

CHOYANG THERMAL MASSAGER

K-Number: K111941 · 2012-05-25

Decision Date2012-05-25
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CHOYANG THERMAL MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Choyang Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2012-05-25 under 510(k) number K111941. 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 CHOYANG THERMAL MASSAGER?

CHOYANG THERMAL MASSAGER is a medical device that received FDA 510(k) clearance on 2012-05-25. The listed applicant is Choyang Medical Instrument Co., Ltd.. The 510(k) number is K111941.

When did CHOYANG THERMAL MASSAGER receive FDA 510(k) clearance?

CHOYANG THERMAL MASSAGER received FDA 510(k) clearance on 2012-05-25, under 510(k) number K111941.

Who is the listed applicant for CHOYANG THERMAL MASSAGER?

The FDA 510(k) record lists Choyang Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHOYANG THERMAL MASSAGER?

The FDA product code for CHOYANG THERMAL MASSAGER is JFB.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: JFB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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