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FDA 510(k)

REPROCESSES USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPS

K-Number: K022753 · 2002-11-14

Decision Date2002-11-14
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

REPROCESSES USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Services. It received FDA 510(k) clearance on 2002-11-14 under 510(k) number K022753. 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 REPROCESSES USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPS?

REPROCESSES USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPS is a medical device that received FDA 510(k) clearance on 2002-11-14. The listed applicant is Medical Device Services. The 510(k) number is K022753.

When did REPROCESSES USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPS receive FDA 510(k) clearance?

REPROCESSES USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPS received FDA 510(k) clearance on 2002-11-14, under 510(k) number K022753.

Who is the listed applicant for REPROCESSES USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPS?

The FDA 510(k) record lists Medical Device Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REPROCESSES USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPS?

The FDA product code for REPROCESSES USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPS 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 Medical Device Services 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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