REGISTREX 1000 PLUS DIGITAL RADIOGRAPHY— 510(k) K840364
Substantially EquivalentAdvanced Technology Laboratories, Inc.
FDA 510(k) clearance K840364 for REGISTREX 1000 PLUS DIGITAL RADIOGRAPHY, Substantially Equivalent on 1984-03-19. Applicant: Advanced Technology Laboratories, Inc..
Clearance details
- Applicant
- Advanced Technology Laboratories, Inc.
- Product code
- Code JAA
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Adverse events under product code JAA
product code JAA- Other
- 1
- Total
- 1
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.