PARA-PAK MACRO-CON— 510(k) K860034

Substantially Equivalent

Meridian Diagnostics, Inc.

FDA 510(k) clearance K860034 for PARA-PAK MACRO-CON, Substantially Equivalent on 1986-02-21. 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: 1986-01-06
Decision date: 1986-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cincinnati, OH, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.