cobas Strep A Nucleic acid test for use on the cobas Liat System (07341911190); cobas Strep A Quality Control Kit (07402678190)
K260047 is the FDA 510(k) clearance record for cobas Strep A Nucleic acid test for use on the cobas Liat System (07341911190); cobas Strep A Quality Control Kit (07402678190), a class II device, cleared for Roche Molecular Systems, Inc. on under FDA product code PGX (Groups A, C And G Beta-Hemolytic Streptococcus Nucleic Acid Amplification System). FDA's definition for product code PGX reads: "An in vitro diagnostic test for the detection of Group A, C and G beta hemolytic Streptococcus in throat swab specimens from symptomatic patients". As of , FDA records show no recalls naming K260047.
Clearance record
- Decision date
- Received
- (233 days to decision)
- Product code
- PGX Groups A, C And G Beta-Hemolytic Streptococcus Nucleic Acid Amplification System
- Regulation
- 21 CFR 866.2680
- Device class
- Class II
- Review panel
- Microbiology
- Applicant
- Roche Molecular Systems, Inc. 4300 Hacienda Dr., Pleasanton CA
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code PGX
Trailing 12 monthsShow 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 | 1 |
| July 2026 | 0 |
| August 2026 | 1 |
| September 2026 | 0 |
| October 2026 | 0 |
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