IMPRA FLEX GRAFTS (VARIOUS PRODUCT CODE NUMBERS)— 510(k) K924360

Unknown

Impra, Inc.

FDA 510(k) clearance K924360 for IMPRA FLEX GRAFTS (VARIOUS PRODUCT CODE NUMBERS), Unknown on 1992-11-25. Applicant: Impra, Inc.. Device class: 2.

Clearance details

Applicant: Impra, Inc.
Product code: Code DYF
Device class: Class 2
Regulation: 21 CFR 870.3450
Advisory panel: Cardiovascular
Date received: 1992-08-28
Decision date: 1992-11-25
Decision: Unknown
Clearance type: Traditional
Location: Tempe, AZ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DYF

K004012 — IMPRA CARBOFLO EPTFE VASCULAR GRAFTS2001-05-14
K000504 — ADVANTA SUPER SOFT GRAFT2000-03-01
K992958 — ADVANTA GRAFT (<6MM)1999-10-01
K991683 — PTFE RINGED GORE-TEX VASCULAR GRAFT1999-09-08
K992441 — ADVANTA GRAFT1999-08-20

More clearances from Impra, Inc.

K004011 — IMPRA CARBOFLO VASCULAR GRAFT, IMPRA CARBOFLO VASCULAR GRAFTS FOR A-V ACCESS2001-03-27
K991027 — BI-DIRECTIONAL TUNNELER1999-04-22
K983769 — DISTAFLO BYPASS GRAFT1998-12-15
K983861 — DISTAFLO BYPASS GRAFT1998-11-24
K983064 — IMPRA HIGH POROSITY GRAFT1998-11-19

Data sourced from openFDA. This site is unofficial and independent of the FDA.