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TAYLOR PATIENT TRANSFER BOARD

K792247 Class I Traditional
Decision Date
1979-11-30
Sponsor / Applicant
Taylor Medical Equipment

Technical Specification

510(k) Submission ID K792247
Product Code IKX
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5050
Decision Date 1979-11-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TAYLOR PATIENT TRANSFER BOARD received FDA 510(k) clearance under submission number K792247, sponsored by Taylor Medical Equipment. 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 1979-11-30.

Classification & Regulation

This clearance is catalogued under FDA product code IKX and 21 CFR 890.5050, within the Physical Medicine review panel as a Class I device.