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FDA 510(k)

VACUUM ASSISTED CLOSURE

K-Number: K021500 · 2002-12-20

ApplicantKinetic Concepts, Inc.
Decision Date2002-12-20
Product CodeOMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VACUUM ASSISTED CLOSURE is the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Concepts, Inc.. It received FDA 510(k) clearance on 2002-12-20 under 510(k) number K021500. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACUUM ASSISTED CLOSURE?

VACUUM ASSISTED CLOSURE is a medical device that received FDA 510(k) clearance on 2002-12-20. The listed applicant is Kinetic Concepts, Inc.. The 510(k) number is K021500.

When did VACUUM ASSISTED CLOSURE receive FDA 510(k) clearance?

VACUUM ASSISTED CLOSURE received FDA 510(k) clearance on 2002-12-20, under 510(k) number K021500.

Who is the listed applicant for VACUUM ASSISTED CLOSURE?

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

What is the FDA product code for VACUUM ASSISTED CLOSURE?

The FDA product code for VACUUM ASSISTED CLOSURE is OMP.

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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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