LASERFLO BLOOD PERFUSION MONITOR 403— 510(k) K851057
Substantially EquivalentTsi, Inc.
FDA 510(k) clearance K851057 for LASERFLO BLOOD PERFUSION MONITOR 403, Substantially Equivalent on 1985-06-24. Applicant: Tsi, Inc..
Clearance details
- Applicant
- Tsi, Inc.
- Product code
- Code DPW
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Paul, MN, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.