Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

V.A.C.ULTA Negative Pressure Wound Therapy System

K-Number: K203316 · 2021-10-27

Decision Date2021-10-27
Product CodeOMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

V.A.C.ULTA Negative Pressure Wound Therapy System is a medical device manufactured by Kci, A Part of 3M Health Care Business Group. It received FDA 510(k) clearance on 2021-10-27 under approval number K203316. 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.ULTA Negative Pressure Wound Therapy System?

V.A.C.ULTA Negative Pressure Wound Therapy System is a medical device that received FDA 510(k) clearance on 2021-10-27. It is manufactured by Kci, A Part of 3M Health Care Business Group. The 510(k) number is K203316.

When was V.A.C.ULTA Negative Pressure Wound Therapy System approved by the FDA?

V.A.C.ULTA Negative Pressure Wound Therapy System received FDA 510(k) clearance on 2021-10-27, under approval number K203316.

What company makes V.A.C.ULTA Negative Pressure Wound Therapy System?

V.A.C.ULTA Negative Pressure Wound Therapy System is manufactured by Kci, A Part of 3M Health Care Business Group.

What is the FDA product code for V.A.C.ULTA Negative Pressure Wound Therapy System?

The FDA product code for V.A.C.ULTA Negative Pressure Wound Therapy System is OMP.

Related Clinical Trials

Related PubMed Literature

Related Devices (Code: OMP)

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.