PHILIPS SITE VIEW WORKSTATION— 510(k) K960809
Substantially EquivalentPhilips Medical Systems North America, Inc.
FDA 510(k) clearance K960809 for PHILIPS SITE VIEW WORKSTATION, Substantially Equivalent on 1996-04-07. Applicant: Philips Medical Systems North America, Inc..
Clearance details
- Applicant
- Philips Medical Systems North America, Inc.
- Product code
- Code LMD
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shelton, CT, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.