UNO Negative Pressure Wound Therapy System
K-Number: K221891 · 2022-12-14
Device Summary
Frequently Asked Questions
What is the UNO Negative Pressure Wound Therapy System?
UNO Negative Pressure Wound Therapy System is a medical device that received FDA 510(k) clearance on 2022-12-14. The listed applicant is Genadyne Biotechnologies, Inc.. The 510(k) number is K221891.
When did UNO Negative Pressure Wound Therapy System receive FDA 510(k) clearance?
UNO Negative Pressure Wound Therapy System received FDA 510(k) clearance on 2022-12-14, under 510(k) number K221891.
Who is the listed applicant for UNO Negative Pressure Wound Therapy System?
The FDA 510(k) record lists Genadyne Biotechnologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UNO Negative Pressure Wound Therapy System?
The FDA product code for UNO 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 Genadyne Biotechnologies, Inc. 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.