Atlas FDA

IS-VZU IGG TEST SYSTEM

FDA 510(k) clearance K981867 · decided 1998-09-28

Clearance details

K-number
K981867
Device name
IS-VZU IGG TEST SYSTEM
Applicant
Diamedix Corp.
Decision
Substantially Equivalent
Date received
1998-05-28
Decision date
1998-09-28
Days to decision
123 days
Clearance type
Traditional
Product code
LFY
Device class
2
Regulation number
866.3900
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Miami, FL, US
Third-party review
No
Expedited review
No

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RecordFirmDate
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ZEUS SCIENTIFIC, INC VZV IGM ELISA TEST SYSTEM (K070317)Zeus Scientific, Inc.2007-07-05
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ZEUS SCIENTIFIC, INC., ATHENA MULTI-LYTE MMRV IGG TEST SYSTEM. (K051484)Zeus Scientific, Inc.2005-12-05
THE APTUS (AUTOMATED) APPLICATION OF THE VZV IGG ELISA TEST SYSTEM (K984181)Zeus Scientific, Inc.1999-01-22
SERAQUEST VZV IGG (K972295)Quest Intl., Inc.1997-11-05
VZV IGG ELISA TEST SYSTEM (K961012)Zeus Scientific, Inc.1996-07-24
VARICELISA, MODIFICATION (K943843)Biowhittaker Molecular Applications, Inc.1996-03-14
VZV IGG ELISA TEST (K941046)Gull Laboratories, Inc.1995-08-24
VITEK IMMUNODIAGNOSTIC ASSAY SYSTEM (K923122)Biomerieux Vitek, Inc.1992-10-26
SERIOLOGICAL TEST KIT/IGM ANTIBODY VARI-ZOST VIRUS (K914022)Pharmacia Diagnostics, Inc.1992-01-27

Recalls involving this device

No recalls on record reference this clearance.