Company ยท US
Dynarad Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1993 to 2000. 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 |
|---|---|---|---|
| Feb 10, 2000 | K000052 | X-RAY MONOBLOCK, MONOBLOCK XRS-60-330 Dynarad Corp. | ITY |
| May 6, 1998 | K981267 | FACTS MONOBLOCK Dynarad Corp. | IZX |
| Dec 30, 1997 | K973833 | CONTROL, X-RAY DIAGNOSTIC, GENERATOR, HIGH VOLTAGE, ASSEMBLY, TUBE HOUSING DIAGNOSTIC, BEAM LIMITING DEVICE, MANUAL Dynarad Corp. | IZL |
| Feb 8, 1995 | K932356 | NOVA XM2 Dynarad Corp. | IZH |
| Jul 20, 1994 | K941363 | PHANTOM Dynarad Corp. | IZL |
| Jan 31, 1994 | K932353 | HF-110A Dynarad Corp. | IZL |
| Aug 3, 1993 | K932355 | 9150A, 1100F Dynarad Corp. | IZL |
| Jul 23, 1993 | K932354 | 9170, 1170 Dynarad Corp. | IZL |
| Jul 14, 1993 | K931725 | ALPHA II Dynarad Corp. | EHD |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||