Atlas FDA

CMV-COMPLEMENT FIXATION ANTIGEN AND NEGATIVE CONTR

FDA 510(k) clearance K852929 · decided 1985-11-12

Clearance details

K-number
K852929
Device name
CMV-COMPLEMENT FIXATION ANTIGEN AND NEGATIVE CONTR
Applicant
Microbix Biosystems, Inc.
Decision
Substantially Equivalent
Date received
1985-07-09
Decision date
1985-11-12
Days to decision
126 days
Clearance type
Traditional
Product code
GQI
Device class
2
Regulation number
866.3175
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Canada, CA
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
ENZYME LINKED IMMUNOABSORBENT ASSAY, CYTOMEGALOVIRUS (K952254)Pyramid Biological Corp.1995-11-16
CMV IGG HUMAN SERUM CONTROLS (K951800)Pyramid Biological Corp.1995-11-16
CMV EARLY ANTIGEN TEST (K942171)Neogenex1994-06-30
VIRGO (R) CMV-IGG ELISA (K883102)Electro-Nucleonics, Inc.1989-02-08
DETECTADOT SYSTEM 2000 CMV IGG TEST (K875159)Gull Laboratories, Inc.1988-05-06
ENZYGNOST ANTI-CMV IGG TEST (K863488)Behring Diagnostics, Inc.1987-07-20
CMV MICROASSAY (K864420)Diamedix Corp.1987-02-02
THE GOLDEN QUAD TEST (CMV) (K861123)Microbiological Research Corp.1987-02-02
CYTOMEGALOVIRUS IGG EIA TEST KIT (K862705)Labsystems, Inc.1986-10-01
COR DOT CMV (K853989)Cordis Corp.1986-06-13
CYTOTECH CMV IGG EIA (K860493)Cytotech, Inc.1986-05-20
CYTOMEGALOVIRUS (CMV) ELISA TEST SYS. CAT. NO:4530 (K854666)Clinical Sciences, Inc.1986-02-05

Recalls involving this device

No recalls on record reference this clearance.