meddevicedb.com FDA Device Reference

ADJUST-A-TEMP MICRO

K841603 Class II Traditional
Decision Date
1984-12-07
Sponsor / Applicant
Suncoast Medical Manufacturers, Inc.

Technical Specification

510(k) Submission ID K841603
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1984-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADJUST-A-TEMP MICRO received FDA 510(k) clearance under submission number K841603, sponsored by Suncoast Medical Manufacturers, 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 1984-12-07.

Classification & Regulation

This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.