Cleared Traditional

K933587 - IMMUNOCARD ROTAVIRUS

K933587 is an FDA 510(k) clearance for IMMUNOCARD ROTAVIRUS, manufactured by Meridian Diagnostics, Inc.. The device is a Class 1 Microbiology device with product code LIQ cleared through the Traditional 510(k) pathway after a 192-day FDA review.

K933587 · Meridian Diagnostics, Inc. · Microbiology device
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Feb 1994
Decision
192d
Days
Class 1
Risk

K933587 is an FDA 510(k) clearance for the IMMUNOCARD ROTAVIRUS. Classified as Enzyme Linked Immunoabsorbent Assay, Rotavirus (product code LIQ), Class I - General Controls.

Submitted by Meridian Diagnostics, Inc. (Cincinnati, US). The FDA issued a Cleared decision on February 3, 1994 after a review of 192 days - an extended review cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.3405 - 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

FDA 510(k) Submission Details - K933587

510(k) Number K933587 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 26, 1993
Decision Date February 03, 1994
Days to Decision 192 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
90d slower than avg
Panel avg: 102d · This submission: 192d
Pathway characteristics
Predicate-based equivalence.

LIQ Device Classification - Class 1, General Controls

Product Code LIQ Enzyme Linked Immunoabsorbent Assay, Rotavirus
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.3405
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - LIQ Enzyme Linked Immunoabsorbent Assay, Rotavirus

All 27
Devices cleared under the same product code (LIQ) and FDA review panel - the closest regulatory comparables to K933587.
VIDAS ROTAVIRUS ASSAY
K965092 · Biomerieux Vitek, Inc. · May 1997
ROTA-DAN RAPID ROTAVIRUS EIA KIT
K951208 · Eldan Technologies, Ltd. · Feb 1996
DIARLEX ROTA-ADENO
K942286 · Orion Diagnostica, Inc. · Dec 1994
KALLESTAD ROTAVIRUS MICROPLATE
K915137 · Bio-Rad Laboratories, Inc. · Mar 1992
DAKO ELISA ROTAVIRUS KIT- 96 TESTS K440
K912666 · Dako Corp. · Feb 1992
SLIDEX ROTA-KIT 2
K895805 · Vitek Systems, Inc. · Feb 1991