meddevicedb.com FDA Device Reference

COOL CUT

K931429 Class I Traditional
Decision Date
1994-04-29
Sponsor / Applicant
Mitab

Technical Specification

510(k) Submission ID K931429
Product Code HWE
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4820
Decision Date 1994-04-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COOL CUT received FDA 510(k) clearance under submission number K931429, sponsored by Mitab. 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 1994-04-29.

Classification & Regulation

This clearance is catalogued under FDA product code HWE and 21 CFR 878.4820, within the General, Plastic Surgery review panel as a Class I device.