ANGIOFLOW METER, ANGIOFLOW ANTEGRADE CATHETER, ANGIOFLOW RETROGRADE CATHETER, MODELS HVT100, ADT1001, ADT1002— 510(k) K033424
Substantially EquivalentTransonic Systems, Inc.
FDA 510(k) clearance K033424 for ANGIOFLOW METER, ANGIOFLOW ANTEGRADE CATHETER, ANGIOFLOW RETROGRADE CATHETER, MODELS HVT100, ADT1001, ADT1002, Substantially Equivalent on 2003-12-11. Applicant: Transonic Systems, Inc..
Clearance details
- Applicant
- Transonic Systems, Inc.
- Product code
- Code DPW
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Ithaca, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.