Cleared Traditional

K982711 - PREMIER GIARDIA

K982711 is the FDA 510(k) clearance for PREMIER GIARDIA by Meridian Diagnostics, Inc.. It is a Class 2 Microbiology device (product code MHI) cleared through the Traditional 510(k) pathway after a 113-day FDA review.

K982711 · Meridian Diagnostics, Inc. · Microbiology device
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Nov 1998
Decision
113d
Days
Class 2
Risk

K982711 is an FDA 510(k) clearance for the PREMIER GIARDIA. Classified as Giardia Spp. (product code MHI), Class II - Special Controls.

Submitted by Meridian Diagnostics, Inc. (Cincinnati, US). The FDA issued a Cleared decision on November 25, 1998 after a review of 113 days - within the typical 510(k) review window.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.3220 - the FDA microbiology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Microbiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Meridian Diagnostics, Inc. devices

Submission Details

510(k) Number K982711 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 04, 1998
Decision Date November 25, 1998
Days to Decision 113 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
11d slower than avg
Panel avg: 102d · This submission: 113d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code MHI Giardia Spp.
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.3220
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Microbiology devices follow this clearance model.

Regulatory Peers - MHI Giardia Spp.

Devices cleared under the same product code (MHI) and FDA review panel - the closest regulatory comparables to K982711.
GIARDIA II
K033274 · Techlab, Inc. · Nov 2003
TRIAGE,PARASITE PANEL, TRIAGE CRYPTOSPORIDIUM AND ENTAMOEBA HISTOLYTICA, TRIAGE CRYPTOSPORIDIUM AND GIARDIA LAMBLIA
K982245 · Biosite Incorporated · Oct 1998
GIARDIA CELISA
K963135 · Techlab, Inc. · Nov 1996
CRYPTO/GIARDIA-CEL IF TEST
K955897 · Techlab, Inc. · Aug 1996
MERIFLUOR-CRYPTOSPORIDIUM/GIARDIA
K912408 · Meridian Diagnostics, Inc. · Jul 1991