Dynarad Corp.
Deer Park, NY, US
Dynarad Corp. appears in FDA device records in Deer Park, NY. FDA records list 9 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Dynarad Corp. between 1993 and 2000. The busiest year on record is 1993, with 3. The most recent is 2000, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1993 | 3 |
| 1994 | 2 |
| 1995 | 1 |
| 1997 | 1 |
| 1998 | 1 |
| 2000 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K000052 | X-RAY MONOBLOCK, MONOBLOCK XRS-60-330 | ITY | Substantially Equivalent | |
| K981267 | FACTS MONOBLOCK | IZX | Substantially Equivalent | |
| K973833 | CONTROL, X-RAY DIAGNOSTIC, GENERATOR, HIGH VOLTAGE, ASSEMBLY, TUBE HOUSING DIAGNOSTIC, BEAM LIMITING DEVICE, MANUAL | IZL | Substantially Equivalent | |
| K932356 | NOVA XM2 | IZH | Substantially Equivalent | |
| K941363 | PHANTOM | IZL | Substantially Equivalent | |
| K932353 | HF-110A | IZL | Substantially Equivalent | |
| K932355 | 9150A, 1100F | IZL | Substantially Equivalent | |
| K932354 | 9170, 1170 | IZL | Substantially Equivalent | |
| K931725 | ALPHA II | EHD | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain