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SUPERCAIR

K890523 Class II Traditional
Decision Date
1989-02-10
Sponsor / Applicant
Ssi Medical Services, Inc.

Technical Specification

510(k) Submission ID K890523
Product Code INX
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5160
Decision Date 1989-02-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUPERCAIR received FDA 510(k) clearance under submission number K890523, sponsored by Ssi Medical Services, 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 1989-02-10.

Classification & Regulation

This clearance is catalogued under FDA product code INX and 21 CFR 890.5160, within the Physical Medicine review panel as a Class II device.