WITT BIOMEDICAL VX-80— 510(k) K880258

Name: FDA 510(k) clearance K880258
Creator: U.S. Food and Drug Administration
Published: 1988-06-16

Substantially Equivalent

Witt Biomedical Corporation

FDA 510(k) clearance K880258 for WITT BIOMEDICAL VX-80, Substantially Equivalent on 1988-06-16. Applicant: Witt Biomedical Corporation. Device class: 2.

Clearance details

Applicant: Witt Biomedical Corporation
Product code: Code DXG
Device class: Class 2
Regulation: 21 CFR 870.1435
Advisory panel: Cardiovascular
Date received: 1988-01-22
Decision date: 1988-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indian Harbour Bch, FL, US

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