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PARKER MODEL PE

K950377 Class I Traditional
Decision Date
1995-09-06
Sponsor / Applicant
Parker Treadmill Co., Inc.

Technical Specification

510(k) Submission ID K950377
Product Code IOL
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5380
Decision Date 1995-09-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PARKER MODEL PE received FDA 510(k) clearance under submission number K950377, sponsored by Parker Treadmill Co., 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 1995-09-06.

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.