meddevicedb.com FDA Device Reference

MEDISEAL CAMERA COVERS

K810512 Class I Traditional
Decision Date
1981-03-13
Sponsor / Applicant
Janin Group, Inc.

Technical Specification

510(k) Submission ID K810512
Product Code KQM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4160
Decision Date 1981-03-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDISEAL CAMERA COVERS received FDA 510(k) clearance under submission number K810512, sponsored by Janin Group, 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 1981-03-13.

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.