Magna Advanced Technologies, Inc.
Miami, FL, US
Magna Advanced Technologies, Inc. appears in FDA device records in Miami, FL. FDA records list 7 510(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
- 7
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 7 510(k) clearances for Magna Advanced Technologies, Inc. between 1998 and 1999. The busiest year on record is 1998, with 6. The most recent is 1999, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1998 | 6 |
| 1999 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K991819 | MAGNATEK 30 | DQA | Substantially Equivalent | |
| K982907 | MAGNATEK 40 | DQA | Substantially Equivalent | |
| K983114 | MAGNATEK80 | CCK | Substantially Equivalent | |
| K982846 | MTEK-1400 | CCK | Substantially Equivalent | |
| K982405 | MTEK-1000 | DQA | Substantially Equivalent | |
| K981310 | MAGNATEK C-300 | GEI | Substantially Equivalent | |
| K981416 | MAGNATEK ELECTROSURGICAL UNITS MODELS, ESU-10, ESU-15 | GEI | 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