meddevicedb.com FDA Device Reference

MED. DYNAMICS SATICAN VIDEO CAMERA 5410

K843294 Class I Traditional
Decision Date
1984-12-12
Sponsor / Applicant
Medline Industries, Inc.

Technical Specification

510(k) Submission ID K843294
Product Code KQM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4160
Decision Date 1984-12-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MED. DYNAMICS SATICAN VIDEO CAMERA 5410 received FDA 510(k) clearance under submission number K843294, sponsored by Medline Industries, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1984-12-12.

Classification & Regulation

This clearance is catalogued under FDA product code KQM and 21 CFR 878.4160, within the General, Plastic Surgery review panel as a Class I device.