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FDA 510(k)

RELAXOR PERFECT TOUCH AIR MASSAGING SYSTEM

K-Number: K030437 · 2003-04-10

ApplicantSalton, Inc.
Decision Date2003-04-10
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RELAXOR PERFECT TOUCH AIR MASSAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Salton, Inc.. It received FDA 510(k) clearance on 2003-04-10 under 510(k) number K030437. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RELAXOR PERFECT TOUCH AIR MASSAGING SYSTEM?

RELAXOR PERFECT TOUCH AIR MASSAGING SYSTEM is a medical device that received FDA 510(k) clearance on 2003-04-10. The listed applicant is Salton, Inc.. The 510(k) number is K030437.

When did RELAXOR PERFECT TOUCH AIR MASSAGING SYSTEM receive FDA 510(k) clearance?

RELAXOR PERFECT TOUCH AIR MASSAGING SYSTEM received FDA 510(k) clearance on 2003-04-10, under 510(k) number K030437.

Who is the listed applicant for RELAXOR PERFECT TOUCH AIR MASSAGING SYSTEM?

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

What is the FDA product code for RELAXOR PERFECT TOUCH AIR MASSAGING SYSTEM?

The FDA product code for RELAXOR PERFECT TOUCH AIR MASSAGING SYSTEM is IRP.

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 Salton, 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: IRP)

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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