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VAC-LOK IMMOBILIZATION SYSTEM

K935300 Class II Traditional
Decision Date
1994-07-18
Sponsor / Applicant
Medtec, Inc.

Technical Specification

510(k) Submission ID K935300
Product Code IYE
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 1994-07-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VAC-LOK IMMOBILIZATION SYSTEM received FDA 510(k) clearance under submission number K935300, sponsored by Medtec, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1994-07-18.

Classification & Regulation

This clearance is catalogued under FDA product code IYE and 21 CFR 892.5050, within the Radiology review panel as a Class II device.