Company ยท US
Oldelft Corp. of America
FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 1998. Name variants (Inc, Corp, punctuation) are merged.
9510(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 |
|---|---|---|---|
| Apr 17, 1998 | K980296 | OLDELFT DIGIDELCA Oldelft Corp. of America | KPR |
| Oct 8, 1997 | K973219 | AMBER DU Oldelft Corp. of America | KPR |
| May 12, 1995 | K946128 | SIMULIX-HP Oldelft Corp. of America | KPQ |
| Feb 15, 1995 | K950037 | N 800 HF Oldelft Corp. of America | IZO |
| Mar 22, 1994 | K932848 | SIMULIX-MC CT EXTENSION Oldelft Corp. of America | JAK |
| Jan 15, 1993 | K923584 | THERAPAX DXT 300 SERIES 3 Oldelft Corp. of America | JAD |
| Jun 5, 1992 | K914784 | PAPILLION PROCTOSCOPE Oldelft Corp. of America | KQA |
| Jun 28, 1991 | K912466 | OLDELFT SIMULIX-MC Oldelft Corp. of America | KPQ |
| Nov 21, 1989 | K892659 | ELECTRODELCA Oldelft Corp. of America | IZG |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||