AUTOLYZER 801 SYSTEM (AUTOMATED CELL COUNTER)— 510(k) K875346
Substantially EquivalentContraves Medical Instruments, Inc.
FDA 510(k) clearance K875346 for AUTOLYZER 801 SYSTEM (AUTOMATED CELL COUNTER), Substantially Equivalent on 1988-04-07. Applicant: Contraves Medical Instruments, Inc..
Clearance details
- Applicant
- Contraves Medical Instruments, Inc.
- Product code
- Code GKZ
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Billerica, MA, US
Adverse events under product code GKZ
product code GKZ- Malfunction
- 1,205
- Total
- 1,205
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.