Atlas FDA

EBV-VCA IGG ELISA TEST SYSTEM

FDA 510(k) clearance K924091 · decided 1993-01-11

Clearance details

K-number
K924091
Device name
EBV-VCA IGG ELISA TEST SYSTEM
Applicant
Zeus Scientific, Inc.
Decision
Substantially Equivalent
Date received
1992-08-13
Decision date
1993-01-11
Days to decision
151 days
Clearance type
Traditional
Product code
MCD
Device class
1
Regulation number
866.3235
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Raritan, NJ, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
THE APTUS (AUTOMATED) APPLICATION OF THE EBV-VCA IGG ELISA TEST SYSTEM. AN ENZYME LINKED IMMUNOSORBENT ASSAY (ELISA) FOR (K984126)Zeus Scientific, Inc.1999-01-11
EPSTEIN-BARR VIRUS COMBI TEST, EBV COMBI TEST (K933251)Virion (U.S.), Inc.1994-06-13
MERIDIAN EBV-IGG TEST KIT (K925689)Fuller Laboratories, Inc.1993-10-12
MODIFIED ORTHO EBV VCA-IGG ELISA (K920412)Ortho Diagnostic Systems, Inc.1992-06-22
EPSTEIN-BARR VIRUS VCA-IGM ANTIBODY ELISA TEST (K911570)Ortho Diagnostic Systems, Inc.1991-06-10
EPSTEIN-BARR VIRUS VCA-IGG ANTIBODY ELISA TEST (K911571)Ortho Diagnostic Systems, Inc.1991-06-10
EBV IGG ELISA TEST (K910872)Gull Laboratories, Inc.1991-04-12

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
ZEUS ELISA PARVOVIRUS B19 IGM TEST SYSTEM (P150042)Zeus Scientific, Inc.2017-09-19
ZEUS ELISA PARVOVIRUS B19 IGG TEST SYSTEM (P150045)Zeus Scientific, Inc.2017-09-19
FLUORO-CEP (R) PROGESTERONE (P900025/S001)Zeus Scientific, Inc.1992-04-21
FLUORO-CEP (R) PROGESTERONE (P900025/S002)Zeus Scientific, Inc.1992-04-17
FLUORO-CEP (R) PROGESTERONE (P900025)Zeus Scientific, Inc.1990-09-26