Atlas FDA

CMV TEST KIT

FDA 510(k) clearance K801963 · decided 1980-10-23

Clearance details

K-number
K801963
Device name
CMV TEST KIT
Applicant
Immuno-Diagnostic Products, Inc.
Decision
Substantially Equivalent
Date received
1980-08-19
Decision date
1980-10-23
Days to decision
65 days
Clearance type
Traditional
Product code
GQH
Device class
2
Regulation number
866.3175
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Walker, MI, 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
BARTELS CINAKIT CMV ANTIGENEMIA (K982311)Intracel Corp.1998-12-14
CMV ANTIGEN CONTROL SLIDES (K964875)Viral Antigens, Inc.1997-03-18
CYTOMEGALOVIRUS INDIRECT IMMUNOFLUORESCENCE ASSAY (K935809)Light Diagnostics1994-05-05
INDIRECT FLUORESCENT ASSAY FOR (HCMV) (K882835)Stellar Bio Systems, Inc.1988-12-05
FITC MURINE MONOCLONAL ANTI-CMV IGG (K882024)Whittaker Bioproducts, Inc.1988-08-03
ORTHO* CYTOMEGALOVIRUS IDENTIFICATION REAGENT (K881932)Ortho Diagnostic Systems, Inc.1988-08-01
BION CMV-G TEST SYSTEM (K880679)Bion Ent., Ltd.1988-06-03
MICROTRAK CMV CULTURE CONFIRMATION TEST (K880290)Syva Co.1988-04-19
COLORGENE DNA HYBRIDIZATION TEST CMV CONFIRMATION (K872576)Enzo Biochem, Inc.1987-12-04
CYTOMEGALOVIRUS CONTROL SLIDES (K873114)Medical Diagnostic Technologies, Inc.1987-09-25
MONABRITE CYTOMEGALOVIRUS (CMV) IFA KIT (K864565)Serono Diagnostics, Inc.1987-02-19
CYTOMEGALOVIRUS (K843657)Institute Virion , Ltd.1985-09-26

Recalls involving this device

No recalls on record reference this clearance.