Company ยท DE
Stockert GmbH
FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2007. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jun 14, 2007 | K070336 | STOCKERT NEURO N50, MODEL12267 Stockert GmbH, DE | GXD |
| Mar 22, 2007 | K070134 | MODIFICATION TO STIMUPLEX HNS-12, MODEL 4892098 Stockert GmbH, DE | BXN |
| Nov 21, 2006 | K061983 | STIMUPLEX PEN Stockert GmbH, DE | BXN |
| Nov 17, 2005 | K052313 | STIMUPLEX HNS-12, MODEL 4892098 Stockert GmbH, DE | BXN |
| Jun 6, 2001 | K003983 | STIMUPLEX HNS-11 Stockert GmbH, DE | BXN |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||