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FDA 510(k)

WFSI'S REPROCESSED COMPRESSION SLEEVE DEVICES

K-Number: K033615 · 2004-02-13

ApplicantWheaton Franciscan Services Inc., Supply Chain
Decision Date2004-02-13
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WFSI'S REPROCESSED COMPRESSION SLEEVE DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Wheaton Franciscan Services Inc., Supply Chain. It received FDA 510(k) clearance on 2004-02-13 under 510(k) number K033615. 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 WFSI'S REPROCESSED COMPRESSION SLEEVE DEVICES?

WFSI'S REPROCESSED COMPRESSION SLEEVE DEVICES is a medical device that received FDA 510(k) clearance on 2004-02-13. The listed applicant is Wheaton Franciscan Services Inc., Supply Chain. The 510(k) number is K033615.

When did WFSI'S REPROCESSED COMPRESSION SLEEVE DEVICES receive FDA 510(k) clearance?

WFSI'S REPROCESSED COMPRESSION SLEEVE DEVICES received FDA 510(k) clearance on 2004-02-13, under 510(k) number K033615.

Who is the listed applicant for WFSI'S REPROCESSED COMPRESSION SLEEVE DEVICES?

The FDA 510(k) record lists Wheaton Franciscan Services Inc., Supply Chain as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WFSI'S REPROCESSED COMPRESSION SLEEVE DEVICES?

The FDA product code for WFSI'S REPROCESSED COMPRESSION SLEEVE DEVICES is JOW.

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Related Devices (Code: JOW)

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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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