MVP (MULTI-VENDOR PROTOCOL CONVERTOR)— 510(k) K900227

Name: FDA 510(k) clearance K900227
Creator: U.S. Food and Drug Administration
Published: 1990-02-12

Substantially Equivalent

Merge Technologies, Inc.

FDA 510(k) clearance K900227 for MVP (MULTI-VENDOR PROTOCOL CONVERTOR), Substantially Equivalent on 1990-02-12. Applicant: Merge Technologies, Inc.. Device class: 1.

Clearance details

Applicant: Merge Technologies, Inc.
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1990-01-17
Decision date: 1990-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milwaukee, WI, US

Download summary PDF View on FDA.gov ↗

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