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FDA 510(k)

HEALTH O METER ELECTRIC HEATING PAD W/MASSAGE MODEL EHP4

K-Number: K962252 · 1996-11-25

Decision Date1996-11-25
Product CodeIRT
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HEALTH O METER ELECTRIC HEATING PAD W/MASSAGE MODEL EHP4 is the device name listed in this FDA 510(k) record. The listed applicant is Sunbeam Health Division. It received FDA 510(k) clearance on 1996-11-25 under 510(k) number K962252. The device is classified under product code IRT. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEALTH O METER ELECTRIC HEATING PAD W/MASSAGE MODEL EHP4?

HEALTH O METER ELECTRIC HEATING PAD W/MASSAGE MODEL EHP4 is a medical device that received FDA 510(k) clearance on 1996-11-25. The listed applicant is Sunbeam Health Division. The 510(k) number is K962252.

When did HEALTH O METER ELECTRIC HEATING PAD W/MASSAGE MODEL EHP4 receive FDA 510(k) clearance?

HEALTH O METER ELECTRIC HEATING PAD W/MASSAGE MODEL EHP4 received FDA 510(k) clearance on 1996-11-25, under 510(k) number K962252.

Who is the listed applicant for HEALTH O METER ELECTRIC HEATING PAD W/MASSAGE MODEL EHP4?

The FDA 510(k) record lists Sunbeam Health Division as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEALTH O METER ELECTRIC HEATING PAD W/MASSAGE MODEL EHP4?

The FDA product code for HEALTH O METER ELECTRIC HEATING PAD W/MASSAGE MODEL EHP4 is IRT.

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 Sunbeam Health Division 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: IRT)

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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