PARA-PAK PVA— 510(k) K792714

Substantially Equivalent

Meridian Diagnostics, Inc.

FDA 510(k) clearance K792714 for PARA-PAK PVA, Substantially Equivalent on 1980-01-24. Applicant: Meridian Diagnostics, Inc.. Device class: 1.

Clearance details

Applicant: Meridian Diagnostics, Inc.
Product code: Code IFQ
Device class: Class 1
Regulation: 21 CFR 864.4010
Advisory panel: Pathology
Date received: 1979-12-27
Decision date: 1980-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IFQ

K792654 — CULTURETTE BRAND-PVA/FORMALIN KIT1980-01-24

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