Eosolutions, Corp.
Eosolutions, Corp. appears in FDA public data with 0 recalls, 1 510(k) clearance, 1 FDA inspection, and 0 compliance actions on record. Its most recent FDA inspection ended on Dec 7, 2023 (Voluntary Action Indicated (VAI)). Its most recent 510(k) clearance was granted on Oct 31, 2023.
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Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 1
- Compliance Actions
- 0
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Dec 7, 2023 | Miramar, FL | Devices | Voluntary Action Indicated (VAI) | 3025028711 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K231629 | 091 Balloon Guide Catheter | Oct 31, 2023 |