VISI-NEISSERIA— 510(k) K913456

Name: FDA 510(k) clearance K913456
Creator: U.S. Food and Drug Administration
Published: 1991-10-11

Substantially Equivalent

Kev Connecticut Diagnostics, Inc.

FDA 510(k) clearance K913456 for VISI-NEISSERIA, Substantially Equivalent on 1991-10-11. Applicant: Kev Connecticut Diagnostics, Inc.. Device class: 1.

Clearance details

Applicant: Kev Connecticut Diagnostics, Inc.
Product code: Code JSX
Device class: Class 1
Regulation: 21 CFR 866.2660
Advisory panel: Microbiology
Date received: 1991-08-05
Decision date: 1991-10-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Danielson, CT, US

Download summary PDF View on FDA.gov ↗

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