PHILIPS ANGIOPRO RELEASE 2.1— 510(k) K933791
Substantially EquivalentPhilips Medical Systems North America, Inc.
FDA 510(k) clearance K933791 for PHILIPS ANGIOPRO RELEASE 2.1, Substantially Equivalent on 1993-11-22. Applicant: Philips Medical Systems North America, Inc..
Clearance details
- Applicant
- Philips Medical Systems North America, Inc.
- Product code
- Code JAA
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shelton, CT, 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.