LIGHTLINE-M— 510(k) K974240

Substantially Equivalent

Wuestec Medical, Inc.

FDA 510(k) clearance K974240 for LIGHTLINE-M, Substantially Equivalent on 1997-12-22. Applicant: Wuestec Medical, Inc.. Device class: 2.

Clearance details

Applicant: Wuestec Medical, Inc.
Product code: Code IZX
Device class: Class 2
Regulation: 21 CFR 892.1610
Advisory panel: Radiology
Date received: 1997-11-12
Decision date: 1997-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mobile, AL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.