MODIFIED VAS-CATH CATHETER REPAIR KIT— 510(k) K890099
Substantially EquivalentVas-Cath, Inc.
FDA 510(k) clearance K890099 for MODIFIED VAS-CATH CATHETER REPAIR KIT, Substantially Equivalent on 1989-04-11. Applicant: Vas-Cath, Inc..
Clearance details
- Applicant
- Vas-Cath, Inc.
- Product code
- Code LFJ
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mississauga, Ontario, CA
Data sourced from openFDA. This site is unofficial and independent of the FDA.