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FDA 510(k)

V.A.C. DERMATAC Drape

K-Number: K181505 · 2019-03-28

ApplicantKci USA, Inc.
Decision Date2019-03-28
Product CodeOMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

V.A.C. DERMATAC Drape is a medical device manufactured by Kci USA, Inc.. It received FDA 510(k) clearance on 2019-03-28 under approval number K181505. 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 V.A.C. DERMATAC Drape?

V.A.C. DERMATAC Drape is a medical device that received FDA 510(k) clearance on 2019-03-28. It is manufactured by Kci USA, Inc.. The 510(k) number is K181505.

When was V.A.C. DERMATAC Drape approved by the FDA?

V.A.C. DERMATAC Drape received FDA 510(k) clearance on 2019-03-28, under approval number K181505.

What company makes V.A.C. DERMATAC Drape?

V.A.C. DERMATAC Drape is manufactured by Kci USA, Inc..

What is the FDA product code for V.A.C. DERMATAC Drape?

The FDA product code for V.A.C. DERMATAC Drape is OMP.

Other Devices by Kci USA, Inc.

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Related Devices (Code: OMP)

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.