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OB TRIPP TRANSPORT CHAIR

K830850 Class I Traditional
Decision Date
1983-04-05
Sponsor / Applicant
Lic-Orthion

Technical Specification

510(k) Submission ID K830850
Product Code INM
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3100
Decision Date 1983-04-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OB TRIPP TRANSPORT CHAIR received FDA 510(k) clearance under submission number K830850, sponsored by Lic-Orthion. 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 1983-04-05.

Classification & Regulation

This clearance is catalogued under FDA product code INM and 21 CFR 890.3100, within the Physical Medicine review panel as a Class I device.