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truFreeze Rapid AV Spray Kit

K171522 Class II Traditional
Decision Date
2017-07-14
Sponsor / Applicant
CSA Medical, Inc.

Technical Specification

510(k) Submission ID K171522
Product Code GEH
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4350
Decision Date 2017-07-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

truFreeze Rapid AV Spray Kit received FDA 510(k) clearance under submission number K171522, sponsored by CSA Medical, Inc.. 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 2017-07-14.

Classification & Regulation

This clearance is catalogued under FDA product code GEH and 21 CFR 878.4350, within the General, Plastic Surgery review panel as a Class II device.