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FDA 510(k)

MOTOR MASSAGE PILLOW

K-Number: K912479 · 1991-08-09

Decision Date1991-08-09
Product CodeIRO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MOTOR MASSAGE PILLOW is the device name listed in this FDA 510(k) record. The listed applicant is Supreme Import , Ltd.. It received FDA 510(k) clearance on 1991-08-09 under 510(k) number K912479. 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 MOTOR MASSAGE PILLOW?

MOTOR MASSAGE PILLOW is a medical device that received FDA 510(k) clearance on 1991-08-09. The listed applicant is Supreme Import , Ltd.. The 510(k) number is K912479.

When did MOTOR MASSAGE PILLOW receive FDA 510(k) clearance?

MOTOR MASSAGE PILLOW received FDA 510(k) clearance on 1991-08-09, under 510(k) number K912479.

Who is the listed applicant for MOTOR MASSAGE PILLOW?

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

What is the FDA product code for MOTOR MASSAGE PILLOW?

The FDA product code for MOTOR MASSAGE PILLOW 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.

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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