The RAMP® RSV control swabs are additional external control reagents to be used with RAMP® RSV test kits as part of a routine quality control program
Who Else Makes It
Concentrated in Zhejiang (2), Guangdong (1), elsewhere (1). One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for Ramp® RSV Control Swabs | Listed by | Response Biomedical Corp., Canada |
| FDA product code | GQG |
| Device type | Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus |
| Device class | Class 1 |
| Regulation | 21 CFR 866.3480 |
| Establishment | Repacker / relabeller, Manufacturer |
| 510(k) | K091235 |
| Record published | 2017-08-31 |
| Record revised | 2025-11-14 (version 3) |
Specifications
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 | Special storage condition: Store at 2 to 30 degrees Celsius. Do not freeze. Contents are stable until the expiration date printed on the box. |
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.