Renu Medical Reporcessed Compressible Limb Sleeves

FDA 510(k) K031559 · Renu Medical, Inc.

Substantially Equivalent

510(k) numberK031559

Submission

Device name
Renu Medical Reporcessed Compressible Limb Sleeves
Applicant
Renu Medical, Inc.
Everett, WA, US
Received
May 19, 2003
Decision date
November 12, 2003
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JOW – Sleeve, Limb, Compressible
Device class
Class II (moderate risk)
Regulation
21 CFR 870.5800
Specialty
Cardiovascular

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K081927Renu Medical Oximetry Sensor, Adult, Ped, Inf,NeoNLF · Traditional 02/06/2009SE
K072194Renu Reprocessed Nellcor Oximetry Sensor, Model D-25, N-25NLF · Traditional 11/29/2007SE
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Questions and answers

When was Renu Medical Reporcessed Compressible Limb Sleeves cleared by the FDA?

Renu Medical Reporcessed Compressible Limb Sleeves (K031559) received a 510(k) decision of Substantially Equivalent on November 12, 2003, 177 days after the submission was received.

What is the product code of K031559?

The FDA product code is JOW – Sleeve, Limb, Compressible, a Class II (moderate risk) device regulated under 21 CFR 870.5800.