BION DIRECT IDENTIFICATION CONTROL SLIDE— 510(k) K890616

Name: FDA 510(k) clearance K890616
Creator: U.S. Food and Drug Administration
Published: 1989-02-17

Substantially Equivalent

Bion Ent., Ltd.

FDA 510(k) clearance K890616 for BION DIRECT IDENTIFICATION CONTROL SLIDE, Substantially Equivalent on 1989-02-17. Applicant: Bion Ent., Ltd.. Device class: 1.

Clearance details

Applicant: Bion Ent., Ltd.
Product code: Code LJG
Device class: Class 1
Regulation: 21 CFR 866.2660
Advisory panel: Microbiology
Date received: 1989-02-07
Decision date: 1989-02-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Park Ridge, IL, US

Download summary PDF View on FDA.gov ↗

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