IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT— 510(k) K964877
Substantially Equivalent - Subject to Tracking Reg.Impra, Inc.
FDA 510(k) clearance K964877 for IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT, Substantially Equivalent - Subject to Tracking Reg. on 1997-03-20. Applicant: Impra, Inc..
Clearance details
- Applicant
- Impra, Inc.
- Product code
- Code DYF
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent - Subject to Tracking Reg.
- Clearance type
- Traditional
- Location
- Tempe, AZ, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.