510(k) DEN140004

Device
QUIDEL MOLECULAR DIRECT HSV 1 +2/VZV ASSAY
Applicant
Diagnostic Hybrids, Inc.
510(k) number
DEN140004
Product code
PGI
Decision
Unknown (DENG)
Decision date
2014-05-13
Date received
2014-02-21
Regulation
866.3309
Classification name
Herpes Virus (Vzv, Hsv1, Hsv2), Dna Detection Assay For Cutaneous And Mucocutaneous Lesion Samples
Medical specialty
Microbiology
Review panel
Microbiology
Device class
2
Clearance type
Post-NSE
Third party reviewed
N

Applicant Contact#

Contact
Ronald H Lollar
Address
2005 E. State St., Suite 100 Athens OH US 45701 45701

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code PGI#

510(k), Device, Applicant table
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