Silaris RSV Control Kit
The Silaris RSV Control Kit is intended for in vitro diagnostic use in quality control testing with the Silaris RSV Test
1manufacturer
1catalogue number
1510(k) clearance
Who Else Makes It
Registered in Guangdong. One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Hochuen Medical Technology Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 20 |
Record
| Listed by | Mesa Biotech, Inc., United States |
|---|---|
| FDA product code | OCC |
| Device type | Respiratory Virus Panel Nucleic Acid Assay System |
| Device class | Class 2 |
| Regulation | 21 CFR 866.3980 |
| Record published | 2019-07-29 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Single use | Yes |
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date |
| Storage | Storage environment temperature 15 to 30 °C; Storage environment temperature 59 to 86 °F |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 1029 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Panther Fusion® | Hologic, Inc. | 4 |
| Prodesse | Hologic, Inc. | 4 |
| Solana | Diagnostic Hybrids, Inc. | 2 |
| Alere™ i Influenza A & B Control Swab Kit | Alere Scarborough, Inc. | 1 |
| Silaris RSV Supplemental Pack | Mesa Biotech, Inc. | 1 |
| Alere i RSV Control Swab Kit | Alere Scarborough, Inc. | 1 |
| ID NOW Influenza A & B 2 Control Swab Kit | Alere Scarborough, Inc. | 1 |
| Xpert Xpress Flu/RSV | Cepheid | 1 |
| ID NOW Influenza A & B Control Swab Kit | Alere Scarborough, Inc. | 1 |
| Simplexa™ Flu A/B & RSV Direct | DiaSorin Molecular LLC | 1 |
| Alere™ i Influenza A & B | Alere Scarborough, Inc. | 1 |
| Respiratory Virus Plus (RV+) Amplification Tray | Nanosphere, Inc. | 1 |
Showing 12 of 39. All products under Respiratory Virus Panel Nucleic Acid Assay System
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K181443 | 2018-11-23 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.