MAUDE report
MAUDE report 4438: ARGON-KRYPTON LASER
No Answer Provided · received Jul 1, 1992 · ALCON SURGICAL INC.
Key facts
| MDR report key | 4438 |
|---|---|
| Report number | 4438 |
| Event type | No Answer Provided |
| Brand name | ARGON-KRYPTON LASER |
| Model number | ALCON 8065-6611-01 OPTHALAS |
| Manufacturer | ALCON SURGICAL INC. |
| Product code | LLF |
| Device class | Class III |
| Date received by FDA | Jul 1, 1992 |
| Report date | Jun 24, 1992 |
| Report source | Maude |
At a glance
- None Device problems coded
- 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: