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LASER BACKPOINTER ASSEMBLY, MOD. 01-2487

K800489 Class I Traditional
Decision Date
1980-03-25
Sponsor / Applicant
Atc Medical Technology, Inc.

Technical Specification

510(k) Submission ID K800489
Product Code IWE
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5780
Decision Date 1980-03-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LASER BACKPOINTER ASSEMBLY, MOD. 01-2487 received FDA 510(k) clearance under submission number K800489, sponsored by Atc Medical Technology, 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 1980-03-25.

Classification & Regulation

This clearance is catalogued under FDA product code IWE and 21 CFR 892.5780, within the Radiology review panel as a Class I device.