Pulmodyne
Pulmodyne appears in FDA public data with 0 recalls, 1 510(k) clearance, 5 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 9, 2008.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 5
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K080256 | PULMODYNE CHF FLOW GENERATOR SYSTEM | May 9, 2008 |