Stockert GmbH
FDA Regulatory Profile
Stockert GmbH appears in FDA public data with 0 recalls, 5 510(k) clearances, 3 FDA inspections, and 1 compliance action on record. Its most recent 510(k) clearance was granted on June 14, 2007.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 3
- Compliance Actions
- 1
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K070336 | STOCKERT NEURO N50, MODEL12267 | June 14, 2007 |
| K070134 | MODIFICATION TO STIMUPLEX HNS-12, MODEL 4892098 | March 22, 2007 |
| K061983 | STIMUPLEX PEN | November 21, 2006 |
| K052313 | STIMUPLEX HNS-12, MODEL 4892098 | November 17, 2005 |
| K003983 | STIMUPLEX HNS-11 | June 6, 2001 |