PARA-PAK SPINCON— 510(k) K980077

Substantially Equivalent

Meridian Diagnostics, Inc.

FDA 510(k) clearance K980077 for PARA-PAK SPINCON, Substantially Equivalent on 1998-04-02. Applicant: Meridian Diagnostics, Inc.. Device class: 1.

Clearance details

Applicant: Meridian Diagnostics, Inc.
Product code: Code LKS
Device class: Class 1
Regulation: 21 CFR 866.2900
Advisory panel: Microbiology
Date received: 1998-01-08
Decision date: 1998-04-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cincinnati, OH, US

Download summary PDF View on FDA.gov ↗

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