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SHOULDER RETRACTOR

K944613 Class II Traditional
Decision Date
1995-01-18
Sponsor / Applicant
Northwest Medical Physics Center

Technical Specification

510(k) Submission ID K944613
Product Code KPR
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1680
Decision Date 1995-01-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SHOULDER RETRACTOR received FDA 510(k) clearance under submission number K944613, sponsored by Northwest Medical Physics Center. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1995-01-18.

Classification & Regulation

This clearance is catalogued under FDA product code KPR and 21 CFR 892.1680, within the Radiology review panel as a Class II device.