meddevicedb.com FDA Device Reference

COMFICARE PAD (FOR SINGEL PT USE)

K792001 Class II Traditional
Decision Date
1979-10-26
Sponsor / Applicant
Hamilton Industries, Inc.

Technical Specification

510(k) Submission ID K792001
Product Code FNM
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5550
Decision Date 1979-10-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMFICARE PAD (FOR SINGEL PT USE) received FDA 510(k) clearance under submission number K792001, sponsored by Hamilton Industries, 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 1979-10-26.

Classification & Regulation

This clearance is catalogued under FDA product code FNM and 21 CFR 880.5550, within the General Hospital review panel as a Class II device.