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FDA 510(k)

STERILMED REPROCESSED COMPRESSION SLEEVES

K-Number: K012597 · 2002-02-11

ApplicantSterilmed, Inc.
Decision Date2002-02-11
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STERILMED REPROCESSED COMPRESSION SLEEVES is the device name listed in this FDA 510(k) record. The listed applicant is Sterilmed, Inc.. It received FDA 510(k) clearance on 2002-02-11 under 510(k) number K012597. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILMED REPROCESSED COMPRESSION SLEEVES?

STERILMED REPROCESSED COMPRESSION SLEEVES is a medical device that received FDA 510(k) clearance on 2002-02-11. The listed applicant is Sterilmed, Inc.. The 510(k) number is K012597.

When did STERILMED REPROCESSED COMPRESSION SLEEVES receive FDA 510(k) clearance?

STERILMED REPROCESSED COMPRESSION SLEEVES received FDA 510(k) clearance on 2002-02-11, under 510(k) number K012597.

Who is the listed applicant for STERILMED REPROCESSED COMPRESSION SLEEVES?

The FDA 510(k) record lists Sterilmed, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILMED REPROCESSED COMPRESSION SLEEVES?

The FDA product code for STERILMED REPROCESSED COMPRESSION SLEEVES is JOW.

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Related Devices (Code: JOW)

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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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