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KEVO NPWT-AHEMO30 AND A HEMO45 FOAM DRESSING KIT

K113199 Class II Traditional
Decision Date
2012-07-30
Sponsor / Applicant
Kevo Medical Supplies

Technical Specification

510(k) Submission ID K113199
Product Code OMP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4780
Decision Date 2012-07-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KEVO NPWT-AHEMO30 AND A HEMO45 FOAM DRESSING KIT received FDA 510(k) clearance under submission number K113199, sponsored by Kevo Medical Supplies. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2012-07-30.

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.