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QuikClot Control+ Hemostatic Dressing

K220971 Class II Traditional
Decision Date
2022-12-14
Sponsor / Applicant
Z-Medica, LLC

Technical Specification

510(k) Submission ID K220971
Product Code POD
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4454
Decision Date 2022-12-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QuikClot Control+ Hemostatic Dressing received FDA 510(k) clearance under submission number K220971, sponsored by Z-Medica, LLC. 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 2022-12-14.

Classification & Regulation

This clearance is catalogued under FDA product code POD and 21 CFR 878.4454, within the General, Plastic Surgery review panel as a Class II device.