meddevicedb.com FDA Device Reference

INDICATOR, BIPOLAR TEMPERATURE

K782043 Class II Traditional
Decision Date
1979-01-17
Sponsor / Applicant
Micronex, Inc.

Technical Specification

510(k) Submission ID K782043
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 1979-01-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INDICATOR, BIPOLAR TEMPERATURE received FDA 510(k) clearance under submission number K782043, sponsored by Micronex, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1979-01-17.

Classification & Regulation

This clearance is catalogued under FDA product code FLL and 21 CFR 880.2910, within the General Hospital review panel as a Class II device.