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REHABILITATION TABLES

K854947 Class I Traditional
Decision Date
1986-01-03
Sponsor / Applicant
I-Rep, Inc.

Technical Specification

510(k) Submission ID K854947
Product Code INQ
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3760
Decision Date 1986-01-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REHABILITATION TABLES received FDA 510(k) clearance under submission number K854947, sponsored by I-Rep, 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 1986-01-03.

Classification & Regulation

This clearance is catalogued under FDA product code INQ and 21 CFR 890.3760, within the Physical Medicine review panel as a Class I device.