Impra, Inc.
Impra, Inc. holds FDA 510(k) medical device clearances, first cleared 1979, most recent 2001.
Top product codes for Impra, Inc.
Recent clearances by Impra, Inc.
- K004012 — IMPRA CARBOFLO EPTFE VASCULAR GRAFTS
- K004011 — IMPRA CARBOFLO VASCULAR GRAFT, IMPRA CARBOFLO VASCULAR GRAFTS FOR A-V ACCESS
- K991027 — BI-DIRECTIONAL TUNNELER
- K983769 — DISTAFLO BYPASS GRAFT
- K983861 — DISTAFLO BYPASS GRAFT
- K983064 — IMPRA HIGH POROSITY GRAFT
- K981076 — VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT
- K981079 — VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT
- K971192 — IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT
- K964877 — IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT
- K964197 — IMPRA CARBOFLO EPTFE VASCULAR GRAFT
- K962639 — IMPRA CARBOFLO EPTFE VASCULAR GRAFT
- K925827 — IMPRAFLO(TM) POST OPERATIVE/DRAIN/REINFUS KIT/CANI
- K924360 — IMPRA FLEX GRAFTS (VARIOUS PRODUCT CODE NUMBERS)
- K915577 — IMPRAFLO POSTOPERATIVE AUTOTRANSFUSION DEVICE
- K905073 — CARDIOVASCULAR REPAIR PATCH
- K904515 — IMPRAFLO 3500 SERIES
- K901232 — IMPRAFLO AUTOTRANSFUSION DEVICE
- K900311 — ARTERIAL EMBOLECTOMY CATHETER
- K901133 — DURACATH
- K892819 — AUTOTRANSFUSION DEVICE
- K883592 — IMPRA DUAL LUMEN SUBCLAVIAN - FEMORAL CATHETER
- K874738 — 10 AND 12 FRENCH VESSEL DILATORS
- K872163 — IMPRA DUAL LUMEN SUBCLAVIAN CATHETER
- K830543 — VASCULAR GRAFT PROSTHESIS EXPANDED MICR
- K823857 — IMPRA PERITONEAL CATHETER
- K812427 — CARTMILL/BARRY FEEDING TUBE
- K801621 — VASCULAR GRAFT PROSTH. OF EXP. MICRO.
- K791810 — VASCULAR GRAFT PROST. OF EXPANDED PTFE
Data sourced from openFDA. This site is unofficial and independent of the FDA.