MAUDE report
MAUDE report 10509: CLINSTAR VERSION 11.1
No Answer Provided · received Dec 13, 1993 · HUFF, BARRINGTON AND OWENS
Key facts
| MDR report key | 10509 |
|---|---|
| Report number | MW1000095 |
| Event type | No Answer Provided |
| Brand name | CLINSTAR VERSION 11.1 |
| Manufacturer | HUFF, BARRINGTON AND OWENS |
| Product code | LNX |
| Date received by FDA | Dec 13, 1993 |
| Report date | Dec 9, 1993 |
| Report source | Maude |
At a glance
- None Device problems coded
- 100–999 MAUDE reports for this product code
- 1–9 MAUDE reports for this brand
- None Death reports for this brand
- None Injury reports for this brand
- No Adverse event flagged
- Yes Product problem flagged
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About MAUDE medical device reports
MAUDE holds medical device reports (MDRs) of suspected device-associated deaths, serious injuries and malfunctions submitted to the FDA by manufacturers, importers, user facilities and the public. A report alone does not establish that a device caused an event.
Source: U.S. Food and Drug Administration (FDA), MAUDE (Manufacturer and User Facility Device Experience) database · Source date: