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FDA 510(k)

CERAGEM-C THERMAL ACUPRESSURE MASSAGER

K-Number: K040031 · 2004-07-28

Decision Date2004-07-28
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CERAGEM-C THERMAL ACUPRESSURE MASSAGER is the device name listed in this FDA 510(k) record. The listed applicant is Ceragem Co., Ltd.. It received FDA 510(k) clearance on 2004-07-28 under 510(k) number K040031. 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-C THERMAL ACUPRESSURE MASSAGER?

CERAGEM-C THERMAL ACUPRESSURE MASSAGER is a medical device that received FDA 510(k) clearance on 2004-07-28. The listed applicant is Ceragem Co., Ltd.. The 510(k) number is K040031.

When did CERAGEM-C THERMAL ACUPRESSURE MASSAGER receive FDA 510(k) clearance?

CERAGEM-C THERMAL ACUPRESSURE MASSAGER received FDA 510(k) clearance on 2004-07-28, under 510(k) number K040031.

Who is the listed applicant for CERAGEM-C THERMAL ACUPRESSURE MASSAGER?

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

What is the FDA product code for CERAGEM-C THERMAL ACUPRESSURE MASSAGER?

The FDA product code for CERAGEM-C THERMAL ACUPRESSURE 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.

Other records listing Ceragem Co., Ltd. as applicant

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.

View all 7 devices →

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

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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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