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Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Angioscore, Inc. · Predicate Candidate Screening

13 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

47 daysmedian FDA review time
139 days90th percentile
13clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K142983AngioSculpt PTA Scoring Balloon Catheter with HydroCross CoaAngioscore, Inc.2015-03-041390
K133998ANGIOSCULPT PTA SCORING BALLOON WITH HYDROCROSS CAOTINGAngioscore, Inc.2014-04-181130
K122685ANGIOSCULPT PTA SCORING BALLOON CATHETERAngioscore, Inc.2013-01-111330
K112182ANGIOSCULPT PTA SCORING BALLOON CATHETERAngioscore, Inc.2011-08-26290
K110767ANGIOSCULPT PTA SCORING BALLOON CATHETERAngioscore, Inc.2011-04-15280
K101735ANGIOSCULPT PTA SCORING BALLOON CATHETER MODEL 2039-XXYY, 21Angioscore, Inc.2010-07-14230
K100303ANGIOSCULPT PTA SCORING BALLOON CATHETER MODEL 2039-XXYY, 20Angioscore, Inc.2010-03-22470
K091966ANGIOSCULPT PTA SCORING BALLOON CATHETER, MODELS 2076-6040, Angioscore, Inc.2009-07-30290
K082059ANGIOSCULPT PTA SCORING BALLOON CATHETERAngioscore, Inc.2008-08-11210
K081220MODIFICATION TO ANGIOSCULPT PTA SCORING BALLOON CATHETERAngioscore, Inc.2008-05-28280
K080151ANGIOSCULPT PTA SCORING BALLOON CATHETER, MODELS 2076 AND 20Angioscore, Inc.2008-04-25945
K072225ANGIOSCULPT PTA SCORING BALLOON CATHETERAngioscore, Inc.2007-10-12635
K050629ANGIOSCULPT SCORING BALLOON CATHETERAngioscore, Inc.2005-09-021750

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda