Nucletron-Oldelft Corp.
Columbia, MD, US
Nucletron-Oldelft Corp. appears in FDA device records in Columbia, MD. FDA records list 11 510(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
- 11
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 11 510(k) clearances for Nucletron-Oldelft Corp. between 1986 and 1996. The busiest year on record is 1986, with 3. The most recent is 1996, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1986 | 3 |
| 1990 | 1 |
| 1991 | 1 |
| 1992 | 2 |
| 1993 | 2 |
| 1995 | 1 |
| 1996 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K953946 | MICROSELECTRON-HDR VERSION 2 | JAQ | Substantially Equivalent | |
| K953831 | N 800 HF | IZO | Substantially Equivalent | |
| K925956 | MICROSELECTRON - HDR FOR MOBILE ENVIRONMENT | JAQ | Substantially Equivalent | |
| K926407 | MODEL COLE TAB-2 TABLE W/MODEL COLE SFD-2 SPOTFILM | KXJ | Substantially Equivalent | |
| K921991 | PLATO RADIATION THERAPY PLANNING SYSTEM | IYE | Substantially Equivalent | |
| K915622 | PLATO BRACHYTHERAPHY TREATMENT PLANNING SYSTEM | JAQ | Substantially Equivalent | |
| K911612 | NUCLETRON PLANNING SYSTEM | IYE | Substantially Equivalent | |
| K902533 | PULSED SELECTRON | JAQ | Substantially Equivalent | |
| K864210 | MICROSELECTRON-HDR (HIGH DOSE RATE) | JAQ | Substantially Equivalent | |
| K853912 | MICROSELECTION INTERSTITIAL REMOTE AFTERLOAD SYS | JAQ | Substantially Equivalent | |
| K852842 | SELECTRON HDR REMOTE AFTERLOADER | JAQ | 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