MAUDE report
MAUDE report 6268: AKCESS CATH-KIT
Death · received Aug 16, 1993 · NEOSTAR MEDICAL TECHNOLOGIES, INC.
Key facts
| MDR report key | 6268 |
|---|---|
| Report number | 6268 |
| Event type | Death |
| Brand name | AKCESS CATH-KIT |
| Model number | AC-190K |
| Catalog number | 2000-031 |
| Manufacturer | NEOSTAR MEDICAL TECHNOLOGIES, INC. |
| Product code | BSY |
| Device class | Class I |
| PMA or 510(k) number | Device Exempt |
| Date received by FDA | Aug 16, 1993 |
| Report date | Jun 28, 1993 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1,000+ MAUDE reports for this product code
- 1–9 MAUDE reports for this brand
- 1–9 Death reports for this brand
- None Injury reports for this brand
- Yes Adverse event flagged
- No 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: