PHILIPS INTEGRIS ALLURA FLAT DETECTOR RELEASE 1.0— 510(k) K022899
Substantially EquivalentPhilips Medical Systems North America Co.
FDA 510(k) clearance K022899 for PHILIPS INTEGRIS ALLURA FLAT DETECTOR RELEASE 1.0, Substantially Equivalent on 2002-11-22. Applicant: Philips Medical Systems North America Co..
Clearance details
- Applicant
- Philips Medical Systems North America Co.
- Product code
- Code JAA
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bothell, WA, 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.