Angioscore, Inc.
Angioscore, Inc. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2015.
Top product codes for Angioscore, Inc.
Recent clearances by Angioscore, Inc.
- K142983 — AngioSculpt PTA Scoring Balloon Catheter with HydroCross Coating
- K133998 — ANGIOSCULPT PTA SCORING BALLOON WITH HYDROCROSS CAOTING
- K122685 — ANGIOSCULPT PTA SCORING BALLOON CATHETER
- K112182 — ANGIOSCULPT PTA SCORING BALLOON CATHETER
- K110767 — ANGIOSCULPT PTA SCORING BALLOON CATHETER
- K101735 — ANGIOSCULPT PTA SCORING BALLOON CATHETER MODEL 2039-XXYY, 2155-XXYY
- K100303 — ANGIOSCULPT PTA SCORING BALLOON CATHETER MODEL 2039-XXYY, 2076-XXYY, 2092-XXYY, 2105-XXYY
- K091966 — ANGIOSCULPT PTA SCORING BALLOON CATHETER, MODELS 2076-6040, 2092-6040, 2105-6040
- K082059 — ANGIOSCULPT PTA SCORING BALLOON CATHETER
- K081220 — MODIFICATION TO ANGIOSCULPT PTA SCORING BALLOON CATHETER
- K080151 — ANGIOSCULPT PTA SCORING BALLOON CATHETER, MODELS 2076 AND 2039
- K072225 — ANGIOSCULPT PTA SCORING BALLOON CATHETER
- K050629 — ANGIOSCULPT SCORING BALLOON CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.