TRUVEL TZ-3X X-RAY DIGITIZING SCANNER— 510(k) K890970

Name: FDA 510(k) clearance K890970
Creator: U.S. Food and Drug Administration
Published: 1989-05-11

Substantially Equivalent

Truvel Corp.

FDA 510(k) clearance K890970 for TRUVEL TZ-3X X-RAY DIGITIZING SCANNER, Substantially Equivalent on 1989-05-11. Applicant: Truvel Corp.. Device class: 2.

Clearance details

Applicant: Truvel Corp.
Product code: Code LMA
Device class: Class 2
Regulation: 21 CFR 892.2030
Advisory panel: Radiology
Date received: 1989-02-27
Decision date: 1989-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chatsworth, CA, US

Download summary PDF View on FDA.gov ↗

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