cobas Factor II and Factor V Test
K172913 is the FDA 510(k) clearance record for cobas Factor II and Factor V Test, a class II device, cleared for Roche Molecular Systems, Inc. on under FDA product code NPR (Test, Factor Ii G20210a Mutations, Genomic Dna Pcr). FDA's definition for product code NPR reads: "In vitro diagnostic test to detect the Factor II G20210A mutation in genomic DNA, as an aid to diagnosis in the evaluation of patients with suspected thrombophilia". FDA records list 53 510(k) clearances for Roche Molecular Systems, Inc., from to . As of , FDA records show no recalls naming K172913.
Clearance record
- Decision date
- Received
- (109 days to decision)
- Product code
- NPR Test, Factor Ii G20210a Mutations, Genomic Dna Pcr
- Regulation
- 21 CFR 864.7280
- Device class
- Class II
- Review panel
- Hematology
- Applicant
- Roche Molecular Systems, Inc. 4300 Hacienda Dr., Pleasanton CA
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code NPR
Trailing 12 monthsFDA records hold no clearances under product code NPR in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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