Atlas FDA

ZEUS ELISA PARVOVIRUS B19 IGG TEST SYSTEM

FDA premarket approval P150045 · decided 2017-09-19

Approval details

PMA number
P150045
Trade name
ZEUS ELISA PARVOVIRUS B19 IGG TEST SYSTEM
Generic name
ASSAY,ENZYME LINKED IMMUNOSORBENT,PARVOVIRUS B19 IGG
Applicant
Zeus Scientific, Inc.
Date received
2015-11-24
Decision date
2017-09-19
Days to decision
665 days
Decision code
APPR
Product code
MYL
Advisory committee
Microbiology
Expedited review
No
Location
Branchburg, NJ
Statement
Approval for the ZEUS ELISA Parvovirus B19 IgG Test System is intended for the qualitative detection of IgG class antibodies to human parvovirus B19 in human serum including women of childbearing age where there is a suspicion of exposure to human parvovirus B19. The test is also for all symptomatic patients as an aid in the diagnosis of fifth disease (erythema infectiosum). This test is for in vitro diagnostic use only.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
Zeus IFA ANA HEp-2 Test System, Zeus dIFine (K201956)Zeus Scientific, Inc.2022-04-29
ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgG/IgM Test System (K190907)Zeus Scientific, Inc.2019-07-29
ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgG Test System (K191398)Zeus Scientific, Inc.2019-07-29
ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgM Test System (K191240)Zeus Scientific, Inc.2019-07-29
ZEUS ELISA BORRELIA VLSE-1/PEPC10 IGG/IGM TEST SYSTEM (K113397)Zeus Scientific, Inc.2012-07-26
ZEUS ELISA CARDIOLIPIN IGG/IGM/IGA TEST SYSTEM (K102425)Zeus Scientific, Inc.2011-12-12
ZEUS ELISA HSV GG-2 IGG TEST SYSTEM (K103603)Zeus Scientific, Inc.2011-05-20
ZEUS ELISA HSV GC-I IGG TEST SYSTEM (K103363)Zeus Scientific, Inc.2011-04-26