Company ยท DE
Von Zeppelin GmbH
FDA 510(k) clearances and medical device recalls filed under this name, 1990 to 2002. 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 |
|---|---|---|---|
| Jan 25, 2002 | K013091 | ZMM 2000 ZEPPELIN MILLENNIUM MOTORDRILL SYSTEM Von Zeppelin GmbH, DE | HBB |
| Oct 8, 1996 | K954658 | PERNECZKY CLIP APPLIER/REMOVER Von Zeppelin GmbH, DE | HCI |
| Dec 11, 1990 | K903151 | INTERVERTEBRAL DISC RONGEUR Von Zeppelin GmbH, DE | HAE |
| Aug 17, 1990 | K901312 | PERNECZKY ANEURYSM CLIP Von Zeppelin GmbH, DE | HCH |
| Jul 23, 1990 | K901313 | INSTRUMENTS FOR NEUROLOGICAL SURGERY Von Zeppelin GmbH, DE | HAE |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||