PWD Negative Pressure Wound Therapy System
K-Number: K212359 · 2022-09-21
Device Summary
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. The listed applicant is Applied Tissue Technologies, LLC. The 510(k) number is K212359.
When did PWD Negative Pressure Wound Therapy System receive FDA 510(k) clearance?
PWD Negative Pressure Wound Therapy System received FDA 510(k) clearance on 2022-09-21, under 510(k) number K212359.
Who is the listed applicant for PWD Negative Pressure Wound Therapy System?
The FDA 510(k) record lists Applied Tissue Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.
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
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Applied Tissue Technologies, LLC as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OMP)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.