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FDA 510(k)

KENDALL SCD SEQUENTIAL COMPRESSION COMFORT SLEEVES

K-Number: K100306 · 2010-05-04

ApplicantCovidien
Decision Date2010-05-04
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

KENDALL SCD SEQUENTIAL COMPRESSION COMFORT SLEEVES is the device name listed in this FDA 510(k) record. The listed applicant is Covidien. It received FDA 510(k) clearance on 2010-05-04 under 510(k) number K100306. 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 KENDALL SCD SEQUENTIAL COMPRESSION COMFORT SLEEVES?

KENDALL SCD SEQUENTIAL COMPRESSION COMFORT SLEEVES is a medical device that received FDA 510(k) clearance on 2010-05-04. The listed applicant is Covidien. The 510(k) number is K100306.

When did KENDALL SCD SEQUENTIAL COMPRESSION COMFORT SLEEVES receive FDA 510(k) clearance?

KENDALL SCD SEQUENTIAL COMPRESSION COMFORT SLEEVES received FDA 510(k) clearance on 2010-05-04, under 510(k) number K100306.

Who is the listed applicant for KENDALL SCD SEQUENTIAL COMPRESSION COMFORT SLEEVES?

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

What is the FDA product code for KENDALL SCD SEQUENTIAL COMPRESSION COMFORT SLEEVES?

The FDA product code for KENDALL SCD SEQUENTIAL COMPRESSION COMFORT 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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