meddevicedb.com FDA Device Reference

Nisus NPWT Canister 500-mL (CPC-500)

K261291 Class II Special
Decision Date
2026-05-21
Sponsor / Applicant
Cork Medical

Technical Specification

510(k) Submission ID K261291
Product Code OMP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4780
Decision Date 2026-05-21
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Nisus NPWT Canister 500-mL (CPC-500) received FDA 510(k) clearance under submission number K261291, sponsored by Cork Medical. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2026-05-21.

Classification & Regulation

This clearance is catalogued under FDA product code OMP and 21 CFR 878.4780, within the General, Plastic Surgery review panel as a Class II device.