Cleared Traditional

PREMIER TYPE SPECIFIC HSV-1 IGG ELISA TEST

K984343 · Meridian Diagnostics, Inc. · Microbiology

Jun 1999

Decision

203d

Days

Class 2

Risk

About This 510(k) Submission

K984343 is an FDA 510(k) clearance for the PREMIER TYPE SPECIFIC HSV-1 IGG ELISA TEST, a Enzyme Linked Immunosorbent Assay, Herpes Simplex Virus, Hsv-1 (Class II — Special Controls, product code MXJ), submitted by Meridian Diagnostics, Inc. (Cincinnati, US). The FDA issued a Cleared decision on June 25, 1999, 203 days after receiving the submission on December 4, 1998. This device falls under the Microbiology review panel. Regulated under 21 CFR 866.3305.

Submission Details

510(k) Number	K984343 FDA.gov
FDA Decision	Cleared SESE
Date Received	December 04, 1998
Decision Date	June 25, 1999
Days to Decision	203 days
Submission Type	Traditional
Review Panel	Microbiology (MI)
Summary	Summary PDF

Device Classification

Product Code	MXJ — Enzyme Linked Immunosorbent Assay, Herpes Simplex Virus, Hsv-1
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 866.3305