IKONISCOPE ONCOFISH BLADDER TEST SYSTEM— 510(k) K062755
Substantially EquivalentIkonisys, Inc.
FDA 510(k) clearance K062755 for IKONISCOPE ONCOFISH BLADDER TEST SYSTEM, Substantially Equivalent on 2007-01-04. Applicant: Ikonisys, Inc..
Clearance details
- Applicant
- Ikonisys, Inc.
- Product code
- Code JOY
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New Haven, CT, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.