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AngioScore Inc.

7 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
AngioScore, Inc. AngioSculpt PTA Scoring Balloon Catheter; OTW 0.018" Platform, 137 cm, 4. recall (Z-0838-2011)AngioScore Inc.2011-01-04
AngioScore, Inc. AngioSculpt PTA Scoring Balloon Catheter; OTW 0.018" Platform, 137 cm, 5. recall (Z-0839-2011)AngioScore Inc.2011-01-04
AngioScore, Inc. AngioSculpt PTA Scoring Balloon Catheter; OTW 0.018" Platform, 137 cm, 6. recall (Z-0840-2011)AngioScore Inc.2011-01-04
AngioScore, Inc. AngioSculpt PTA Scoring Balloon Catheter; OTW 0.018" Platform, 90 cm, 6.0 recall (Z-0841-2011)AngioScore Inc.2011-01-04
AngioScore, Inc. AngioSculpt PTA Scoring Balloon Catheter; OTW 0.018" Platform, 50 cm, 6.0 recall (Z-0842-2011)AngioScore Inc.2011-01-04
AngioSculpt Percutaneous Transluminal Coronary Angioplasty (PTCA) Catheter, cutting/scorin recall (Z-2218-2010)AngioScore Inc.2010-08-18
AngioSculpt PTCA Scoring Balloon Catheter, Catalog (REF) Number: 2027-2510, size 2.5mm x 1 recall (Z-0591-2008)AngioScore Inc.2008-01-23

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Every clearance here is in the API, with alerts when new ones post.