Capsule Tech Inc.
FDA Regulatory Profile
Capsule Tech Inc. appears in FDA public data with 1 recall, 1 510(k) clearance, 4 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2377-2012, Class II) was initiated on August 10, 2012. Its most recent 510(k) clearance was granted on June 27, 2012.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 1
- Inspections
- 4
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
| Z-2377-2012 | Class II | Capsule Neuron Docking Station, a component in the DataCaptor Connectivity System Catalog Number DC | August 10, 2012 |
Recent 510(k) Clearances
| K-Number | Device | Date |
| K113835 | DATACAPTOR SYSTEM | June 27, 2012 |