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FDA 510(k)

TCM MASSAGER

K-Number: K130150 · 2013-09-26

Decision Date2013-09-26
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TCM MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Anhui Jinjianqiao Med-Tech Co,. , Ltd.. It received FDA 510(k) clearance on 2013-09-26 under 510(k) number K130150. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TCM MASSAGER?

TCM MASSAGER is a medical device that received FDA 510(k) clearance on 2013-09-26. The listed applicant is Anhui Jinjianqiao Med-Tech Co,. , Ltd.. The 510(k) number is K130150.

When did TCM MASSAGER receive FDA 510(k) clearance?

TCM MASSAGER received FDA 510(k) clearance on 2013-09-26, under 510(k) number K130150.

Who is the listed applicant for TCM MASSAGER?

The FDA 510(k) record lists Anhui Jinjianqiao Med-Tech Co,. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TCM MASSAGER?

The FDA product code for TCM MASSAGER is NUH.

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: NUH)

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

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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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