Phoenix Clinical ICON— 510(k) K170527
Substantially EquivalentPhoenix Technology Group, Inc. Dba Phoenix Clinical
FDA 510(k) clearance K170527 for Phoenix Clinical ICON, Substantially Equivalent on 2017-09-15. Applicant: Phoenix Technology Group, Inc. Dba Phoenix Clinical. Device class: 2.
Clearance details
- Applicant
- Phoenix Technology Group, Inc. Dba Phoenix Clinical
- Product code
- Code HKI
- Device class
- Class 2
- Regulation
- 21 CFR 886.1120
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Pleasanton, CA, US
Recent devices under product code HKI
view allData sourced from openFDA. This site is unofficial and independent of the FDA.