THE X-RAY DIGITIZER, ALTEK MODEL ACT20020-BL— 510(k) K895442

Name: FDA 510(k) clearance K895442
Creator: U.S. Food and Drug Administration
Published: 1989-12-14

Substantially Equivalent

Altek Corp.

FDA 510(k) clearance K895442 for THE X-RAY DIGITIZER, ALTEK MODEL ACT20020-BL, Substantially Equivalent on 1989-12-14. Applicant: Altek Corp.. Device class: 2.

Clearance details

Applicant: Altek Corp.
Product code: Code KPQ
Device class: Class 2
Regulation: 21 CFR 892.5840
Advisory panel: Radiology
Date received: 1989-09-08
Decision date: 1989-12-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Silver Spring, MD, US

Download summary PDF View on FDA.gov ↗

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