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Test 5, 10-Methylenetetrahydrofolate Reductase Mutations, Genomic Dna Pcr

Page Type
Product Code
Definition
In vitro diagnostic for the detection and genotyping of a single point mutation of the human 5, 10-methylenetetrahydrofolate reductase gene (MTHFR) in patients with suspected thrombophilia.
Physical State
genotyping test system
Technical Method
Uses DNA genotyping technology to determine patient genotype at the 5, 10-methylenetetrahydrofolate reductase gene locus.
Target Area
clinical samples (blood, saliva, buccal swab samples)
Regulation Medical Specialty
Hematology
Review Panel
Hematology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
864.7280
GMP Exempt?
No
Summary Malfunction Reporting
Eligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Third Party Eligible

CFR § 864.7280 Factor V Leiden DNA mutation detection systems

§ 864.7280 Factor V Leiden DNA mutation detection systems.

(a) Identification. Factor V Leiden deoxyribonucleic acid (DNA) mutation detection systems are devices that consist of different reagents and instruments which include polymerase chain reaction (PCR) primers, hybridization matrices, thermal cyclers, imagers, and software packages. The detection of the Factor V Leiden mutation aids in the diagnosis of patients with suspected thrombophilia.

(b) Classification. Class II (special controls). The special control is FDA's guidance entitled “Class II Special Controls Guidance Document: Factor V Leiden DNA Mutation Detection Systems.” (See § 864.1(d) for the availability of this guidance document.)

[69 FR 12273, Mar. 16, 2004]

Test 5, 10-Methylenetetrahydrofolate Reductase Mutations, Genomic Dna Pcr

Page Type
Product Code
Definition
In vitro diagnostic for the detection and genotyping of a single point mutation of the human 5, 10-methylenetetrahydrofolate reductase gene (MTHFR) in patients with suspected thrombophilia.
Physical State
genotyping test system
Technical Method
Uses DNA genotyping technology to determine patient genotype at the 5, 10-methylenetetrahydrofolate reductase gene locus.
Target Area
clinical samples (blood, saliva, buccal swab samples)
Regulation Medical Specialty
Hematology
Review Panel
Hematology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
864.7280
GMP Exempt?
No
Summary Malfunction Reporting
Eligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Third Party Eligible

CFR § 864.7280 Factor V Leiden DNA mutation detection systems

§ 864.7280 Factor V Leiden DNA mutation detection systems.

(a) Identification. Factor V Leiden deoxyribonucleic acid (DNA) mutation detection systems are devices that consist of different reagents and instruments which include polymerase chain reaction (PCR) primers, hybridization matrices, thermal cyclers, imagers, and software packages. The detection of the Factor V Leiden mutation aids in the diagnosis of patients with suspected thrombophilia.

(b) Classification. Class II (special controls). The special control is FDA's guidance entitled “Class II Special Controls Guidance Document: Factor V Leiden DNA Mutation Detection Systems.” (See § 864.1(d) for the availability of this guidance document.)

[69 FR 12273, Mar. 16, 2004]