RENU MEDICAL REPORCESSED COMPRESSIBLE LIMB SLEEVES
K-Number: K031559 · 2003-11-12
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Device Summary
Frequently Asked Questions
What is the RENU MEDICAL REPORCESSED COMPRESSIBLE LIMB SLEEVES?
RENU MEDICAL REPORCESSED COMPRESSIBLE LIMB SLEEVES is a medical device that received FDA 510(k) clearance on 2003-11-12. The listed applicant is Renu Medical, Inc.. The 510(k) number is K031559.
When did RENU MEDICAL REPORCESSED COMPRESSIBLE LIMB SLEEVES receive FDA 510(k) clearance?
RENU MEDICAL REPORCESSED COMPRESSIBLE LIMB SLEEVES received FDA 510(k) clearance on 2003-11-12, under 510(k) number K031559.
Who is the listed applicant for RENU MEDICAL REPORCESSED COMPRESSIBLE LIMB SLEEVES?
The FDA 510(k) record lists Renu Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RENU MEDICAL REPORCESSED COMPRESSIBLE LIMB SLEEVES?
The FDA product code for RENU MEDICAL REPORCESSED COMPRESSIBLE LIMB SLEEVES is JOW.
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 Renu Medical, 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: JOW)
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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