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FDA 510(k)

SONIX...THERAPEUTIC SONIC MASSAGE

K-Number: K913439 · 1992-01-22

Decision Date1992-01-22
Product CodeIRO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SONIX...THERAPEUTIC SONIC MASSAGE is the device name listed in this FDA 510(k) record. The listed applicant is Mcshirley Products, Inc.. It received FDA 510(k) clearance on 1992-01-22 under 510(k) number K913439. The device is classified under product code IRO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONIX...THERAPEUTIC SONIC MASSAGE?

SONIX...THERAPEUTIC SONIC MASSAGE is a medical device that received FDA 510(k) clearance on 1992-01-22. The listed applicant is Mcshirley Products, Inc.. The 510(k) number is K913439.

When did SONIX...THERAPEUTIC SONIC MASSAGE receive FDA 510(k) clearance?

SONIX...THERAPEUTIC SONIC MASSAGE received FDA 510(k) clearance on 1992-01-22, under 510(k) number K913439.

Who is the listed applicant for SONIX...THERAPEUTIC SONIC MASSAGE?

The FDA 510(k) record lists Mcshirley Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SONIX...THERAPEUTIC SONIC MASSAGE?

The FDA product code for SONIX...THERAPEUTIC SONIC MASSAGE is IRO.

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 Mcshirley Products, Inc. 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.

Related Devices (Code: IRO)

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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