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Product codes
OAV
Product code OAV
Device name
Mycophenolic Acid Test System
Medical specialty
Clinical Toxicology
Device class
2
Regulation number
862.3840
Review panel
TX
Implant
N
Life sustaining/supporting
N
GMP exempt
N
Third party review
Y
Summary malfunction reporting
Eligible
Definition
An in vitro diagnostic reagent system intended for use in the quantitative determination of total mycophenolic acid in human serum or plasma as an aid in the management of mycophenolic acid therapy in renal and cardiac transplant patients.
Source
FDA openFDA device classification dataset
Related 510(k) Records
#
510(k), Device, Applicant table
510(k)
Device
Applicant
Decision date
K102772
DIMENSION MYCOPHENOLIC ACID (MPAT) FLEX REAGENT CARTRIDGE, DIMENSION MYCOPHENOLIC ACID CALIBRATOR (MPAT CAL)
Siemens Heatlhcare Diagnostics, Inc.
2011-10-07
K081083
CEDIA MYCOPHENOLIC ACID ASSAY, CALIBRATORS, MAS MYCOPHENOLIC ACID CONTROLS
Thermo Fisher Scientific
2008-12-19
K063520
ROCHE TOTAL MYCOPHENOLIC ACID ASSAY, CALIBRATORS AND CONTROLS
Roche Diagnostics
2007-02-16
Related GUDID Devices
#
Primary DI, Brand, Company table
Primary DI
Brand
Company
Published
07613336133675
Mycophenolic Acid
Roche Diagnostics GmbH
2020-03-05
00884883001800
CEDIA Mycophenolic Acid Assay
Microgenics Corporation
2016-09-24
00842768036217
Dimension® Flex® reagent cartridge MPAT
Siemens Healthcare Diagnostics Inc.
2016-09-24
00884883011878
CEDIA Mycophenolic Acid Assay
Microgenics Corporation
2016-09-22
04015630997381
Mycophenolic Acid
Roche Diagnostics GmbH
2016-09-20