MOISTURESTAY (REVLON)
K-Number: K022626 · 2002-10-29
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Device Summary
Frequently Asked Questions
What is the MOISTURESTAY (REVLON)?
MOISTURESTAY (REVLON) is a medical device that received FDA 510(k) clearance on 2002-10-29. The listed applicant is Raymond Industrial, Ltd.. The 510(k) number is K022626.
When did MOISTURESTAY (REVLON) receive FDA 510(k) clearance?
MOISTURESTAY (REVLON) received FDA 510(k) clearance on 2002-10-29, under 510(k) number K022626.
Who is the listed applicant for MOISTURESTAY (REVLON)?
The FDA 510(k) record lists Raymond Industrial, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOISTURESTAY (REVLON)?
The FDA product code for MOISTURESTAY (REVLON) is IMC.
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 Raymond Industrial, Ltd. 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: IMC)
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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