meddevicedb.com FDA Device Reference

SKYLIGHT IMAGING SYSTEM

K000908 Class II Traditional
Decision Date
2000-04-05
Sponsor / Applicant
Adac Laboratories

Technical Specification

510(k) Submission ID K000908
Product Code KPS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1200
Decision Date 2000-04-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SKYLIGHT IMAGING SYSTEM received FDA 510(k) clearance under submission number K000908, sponsored by Adac Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2000-04-05.

Classification & Regulation

This clearance is catalogued under FDA product code KPS and 21 CFR 892.1200, within the Radiology review panel as a Class II device.