ARTHRITIC HEAT WRAP
K-Number: K925820 · 1994-02-02
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Device Summary
Frequently Asked Questions
What is the ARTHRITIC HEAT WRAP?
ARTHRITIC HEAT WRAP is a medical device that received FDA 510(k) clearance on 1994-02-02. The listed applicant is Conair Corp.. The 510(k) number is K925820.
When did ARTHRITIC HEAT WRAP receive FDA 510(k) clearance?
ARTHRITIC HEAT WRAP received FDA 510(k) clearance on 1994-02-02, under 510(k) number K925820.
Who is the listed applicant for ARTHRITIC HEAT WRAP?
The FDA 510(k) record lists Conair Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARTHRITIC HEAT WRAP?
The FDA product code for ARTHRITIC HEAT WRAP 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 Conair Corp. 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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