meddevicedb.com FDA Device Reference

1 VIDEO TAPE RECORDER MODEL BK-224 H

K892934 Class II Traditional
Decision Date
1989-07-20
Sponsor / Applicant
Perkins Mfg. Co.

Technical Specification

510(k) Submission ID K892934
Product Code OXO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1650
Decision Date 1989-07-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

1 VIDEO TAPE RECORDER MODEL BK-224 H received FDA 510(k) clearance under submission number K892934, sponsored by Perkins Mfg. Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1989-07-20.

Classification & Regulation

This clearance is catalogued under FDA product code OXO and 21 CFR 892.1650, within the Radiology review panel as a Class II device.