CONAIR BODY AND SOLE
K-Number: K950410 · 1995-05-23
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Device Summary
Frequently Asked Questions
What is the CONAIR BODY AND SOLE?
CONAIR BODY AND SOLE is a medical device that received FDA 510(k) clearance on 1995-05-23. The listed applicant is Conair Corp.. The 510(k) number is K950410.
When did CONAIR BODY AND SOLE receive FDA 510(k) clearance?
CONAIR BODY AND SOLE received FDA 510(k) clearance on 1995-05-23, under 510(k) number K950410.
Who is the listed applicant for CONAIR BODY AND SOLE?
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 CONAIR BODY AND SOLE?
The FDA product code for CONAIR BODY AND SOLE 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 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: 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
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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