CRITIVIEW— 510(k) K051145
Substantially EquivalentCritisense , Ltd.
FDA 510(k) clearance K051145 for CRITIVIEW, Substantially Equivalent on 2006-01-18. Applicant: Critisense , Ltd..
Clearance details
- Applicant
- Critisense , Ltd.
- Product code
- Code DPW
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mccordsville, IN, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.