Atlas FDA

CMVGEN

FDA 510(k) clearance K974456 · decided 1998-05-01

Clearance details

K-number
K974456
Device name
CMVGEN
Applicant
Instrumentation Laboratory CO
Decision
Substantially Equivalent
Date received
1997-11-25
Decision date
1998-05-01
Days to decision
157 days
Clearance type
Traditional
Product code
LJO
Device class
2
Regulation number
866.3175
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Lexington, MA, 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
Capture-CMV (K203612)Immucor, Inc.2021-03-22
Capture-CMV (K183571)Immucor, Inc.2019-02-04
DIAMEDIX IS-CMV IGM CAPTURE TEST SYSTEM (K001767)Diamedix Corp.2000-08-07
HYBRID CAPTURE SYSTEM CMV DNA ASSAY (K974901)Digene Corp.1998-09-29
ALLIANCE CYTOMEGALOVIRUS IMMEDIATE EARLY ANTIGEN DIRECT IMMUNOFLUORESCENCE ASSAY (K951851)E.I. Dupont DE Nemours & Co., Inc.1996-07-24
COPALIS CMV TOTAL ANTIBODY ASSAY (K955799)Sienna Biotech, Inc.1996-07-10
HEALTHTEST ASSAY FOR ANTIBODY TO CYTOMEGALOVIRUS (K920222)Akers Research Corp.1992-07-27
CYTOMEGALOVIRUS ANTIBODY SCREEN (K910003)Immucor, Inc.1991-03-20
CMV-IHA (K852494)Hillcrest Biologicals1985-09-16
CMV LATEX AGGLUTINATION TEST KIT (K841520)Bd Becton Dickinson Vacutainer Systems Preanalytic1984-09-07
CETUS CMV IHA (K822965)Cetus Corp.1983-02-15

Recalls involving this device

No recalls on record reference this clearance.