Radkor, Inc.
Irvine, CA, US
Radkor, Inc. appears in FDA device records in Irvine, CA. FDA records list 10 510(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
- 10
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 10 510(k) clearances for Radkor, Inc. between 1988 and 1989. The busiest year on record is 1988, with 7. The most recent is 1989, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1988 | 7 |
| 1989 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K895969 | RADKOR DXG-650R | IZO | Substantially Equivalent | |
| K892196 | RADKOR TS10-B | IXQ | Substantially Equivalent | |
| K891395 | RADKOR BS-10 AND BS-10T | IXY | Substantially Equivalent | |
| K883885 | RADKOR, RF-159 | KXJ | Substantially Equivalent | |
| K883864 | RADKOR SFR-70 | IYB | Substantially Equivalent | |
| K881701 | RADKOR SFC-21 | IYB | Substantially Equivalent | |
| K883081 | RADKOR, XG-515 | IZO | Substantially Equivalent | |
| K881700 | RADKOR KOB-84 | KXJ | Substantially Equivalent | |
| K881696 | RADKOR XG-325 | IZO | Substantially Equivalent | |
| K882563 | RADKOR, CST-18 | IYB | 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