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SECUTEX KNEE BAND

K791266 Class I Traditional
Decision Date
1979-07-24
Sponsor / Applicant
Conphar, Inc.

Technical Specification

510(k) Submission ID K791266
Product Code IQI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3475
Decision Date 1979-07-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SECUTEX KNEE BAND received FDA 510(k) clearance under submission number K791266, sponsored by Conphar, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1979-07-24.

Classification & Regulation

This clearance is catalogued under FDA product code IQI and 21 CFR 890.3475, within the Physical Medicine review panel as a Class I device.