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SECURA BATH SEAT

K812483 Class I Traditional
Decision Date
1981-09-14
Sponsor / Applicant
Maddak, Inc.

Technical Specification

510(k) Submission ID K812483
Product Code ILS
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5050
Decision Date 1981-09-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SECURA BATH SEAT received FDA 510(k) clearance under submission number K812483, sponsored by Maddak, 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 1981-09-14.

Classification & Regulation

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