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

FDA 510(k)

WoundPro Negative Pressure Wound Therapy System

K-Number: K150960 · 2016-12-01

Decision Date2016-12-01
Product CodeOMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WoundPro Negative Pressure Wound Therapy System is the device name listed in this FDA 510(k) record. The listed applicant is Pensar Medical, LLC. It received FDA 510(k) clearance on 2016-12-01 under 510(k) number K150960. 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 WoundPro Negative Pressure Wound Therapy System?

WoundPro Negative Pressure Wound Therapy System is a medical device that received FDA 510(k) clearance on 2016-12-01. The listed applicant is Pensar Medical, LLC. The 510(k) number is K150960.

When did WoundPro Negative Pressure Wound Therapy System receive FDA 510(k) clearance?

WoundPro Negative Pressure Wound Therapy System received FDA 510(k) clearance on 2016-12-01, under 510(k) number K150960.

Who is the listed applicant for WoundPro Negative Pressure Wound Therapy System?

The FDA 510(k) record lists Pensar Medical, LLC as the applicant. This does not by itself establish the device manufacturer.

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

The FDA product code for WoundPro 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 Pensar Medical, 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.