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FDA 510(k)

PWD Negative Pressure Wound Therapy System

K-Number: K212359 · 2022-09-21

Decision Date2022-09-21
Product CodeOMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PWD Negative Pressure Wound Therapy System is a medical device manufactured by Applied Tissue Technologies, LLC. It received FDA 510(k) clearance on 2022-09-21 under approval number K212359. 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 PWD Negative Pressure Wound Therapy System?

PWD Negative Pressure Wound Therapy System is a medical device that received FDA 510(k) clearance on 2022-09-21. It is manufactured by Applied Tissue Technologies, LLC. The 510(k) number is K212359.

When was PWD Negative Pressure Wound Therapy System approved by the FDA?

PWD Negative Pressure Wound Therapy System received FDA 510(k) clearance on 2022-09-21, under approval number K212359.

What company makes PWD Negative Pressure Wound Therapy System?

PWD Negative Pressure Wound Therapy System is manufactured by Applied Tissue Technologies, LLC.

What is the FDA product code for PWD Negative Pressure Wound Therapy System?

The FDA product code for PWD Negative Pressure Wound Therapy System is OMP.

Related Clinical Trials

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Official Source

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