Lorad Corp.
Danbury, CT, US
Lorad Corp. appears in FDA device records in Danbury, CT. FDA records list 12 510(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
- 12
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 12 510(k) clearances for Lorad Corp. between 1994 and 1999. The busiest year on record is 1994, with 6. The most recent is 1999, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1994 | 6 |
| 1995 | 3 |
| 1997 | 1 |
| 1998 | 1 |
| 1999 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K992280 | LORAD 1-650 (INTERNATIONAL 650) | IZH | Substantially Equivalent | |
| K974460 | LITE TOUCH ERBIUM LASER TREATMENT SYSTEM | GEX | Substantially Equivalent | |
| K973631 | LORAD M-III ELITE (M-III E) | IZH | Substantially Equivalent | |
| K952210 | LORAD STEROLOC II | IZH | Substantially Equivalent | |
| K945241 | LORAD M-IV, LORAD M-IVI | IZH | Substantially Equivalent | |
| K950608 | DIGITAL SPOT MAMMOGRAPHY FOR STEROTACTIC APPLICATION | IZH | Substantially Equivalent | |
| K945496 | MAMMOGRAPHIC X-RAY UNIT | IZH | Substantially Equivalent | |
| K945272 | RHODIUM FILTER | IZH | Substantially Equivalent | |
| K934868 | LORAD TRANSPO | IZH | Substantially Equivalent | |
| K934870 | LORAD D-550 | IZH | Substantially Equivalent | |
| K934748 | LORAD M-IIE MODIFICATION | IZH | Substantially Equivalent | |
| K934625 | LORAD M-III | IZH | 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