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OHIO HEAT REFLECTING PATCH

K840967 Class II Traditional
Decision Date
1984-03-23
Sponsor / Applicant
Ohio Medical Products

Technical Specification

510(k) Submission ID K840967
Product Code FMI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 1984-03-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OHIO HEAT REFLECTING PATCH received FDA 510(k) clearance under submission number K840967, sponsored by Ohio Medical Products. 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 1984-03-23.

Classification & Regulation

This clearance is catalogued under FDA product code FMI and 21 CFR 880.5570, within the General Hospital review panel as a Class II device.