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PACER R 9 TREADMILL

K893032 Class I Traditional
Decision Date
1989-07-27
Sponsor / Applicant
Pacer Industries, Inc.

Technical Specification

510(k) Submission ID K893032
Product Code IOL
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5380
Decision Date 1989-07-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PACER R 9 TREADMILL received FDA 510(k) clearance under submission number K893032, sponsored by Pacer Industries, 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 1989-07-27.

Classification & Regulation

This clearance is catalogued under FDA product code IOL and 21 CFR 890.5380, within the Physical Medicine review panel as a Class I device.