Viramed Biotech AG
Viramed Biotech AG appears in FDA public data with 0 recalls, 7 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 19, 2022.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K220016 | Viramed Borrela All-In-One ViraChip Test Kit | August 19, 2022 |
| K163695 | Borrelia B31 ViraChip IgM Test Kit | August 22, 2017 |
| K163504 | Borrelia B31 ViraChip IgG Test Kit | July 12, 2017 |
| K092693 | VIRAMED BIOTECH AG BORRELIA B31 IGG VIRASTRIPE, MODEL V-BBSGUS | November 25, 2009 |
| K082329 | VIRAMED BIOTECH AG BORRELIA B31 IGM VIRASTRIPE | August 5, 2009 |
| K051169 | BIRAMED BIOTECH BORRELIA B31 IGM VIRABLOT | August 11, 2005 |
| K051071 | VIRAMED BIOTECH BORRELIA B31 IGG VIRABLOT | August 11, 2005 |