SUPERSTAND 300— 510(k) K935123

Substantially Equivalent

Wuestec Medical, Inc.

FDA 510(k) clearance K935123 for SUPERSTAND 300, Substantially Equivalent on 1996-03-27. Applicant: Wuestec Medical, Inc.. Device class: 1.

Clearance details

Applicant: Wuestec Medical, Inc.
Product code: Code IYB
Device class: Class 1
Regulation: 21 CFR 892.1770
Advisory panel: Radiology
Date received: 1993-10-28
Decision date: 1996-03-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mobile, AL, US

Download summary PDF View on FDA.gov ↗

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K974240 — LIGHTLINE-M1997-12-22

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