Atlas FDA

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

Imperative Care, Inc. — Predicate Candidate Screening

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

66 daysmedian FDA review time
238 days90th percentile
17clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K252046Zoom System (Zoom 4S Catheter)Imperative Care, Inc.2025-10-301220
K252057Symphony™ Thrombectomy System and Symphony™ 16F 82cm ThrombeImperative Care, Inc.2025-08-28580
K244061X-Wire GuidewireImperative Care, Inc.2025-08-262380
K243047Zoom 7X Catheter; Zoom Aspiration Tubing; Zoom POD AspiratioImperative Care, Inc.2025-05-282430
K250775Symphony™ Thrombectomy System; Symphony™ 16F 82cm ThrombectoImperative Care, Inc.2025-05-14610
K242672Zoom SystemImperative Care, Inc.2025-01-141300
K240948TracStar LDP Large Distal Platform; Zoom 88 Large Distal PlaImperative Care, Inc.2024-06-06590
K233975Zoom 6F Insert CathetersImperative Care, Inc.2024-04-021090
K231168TracStar LDP Large Distal Platform; Zoom 88 Large Distal PlaImperative Care, Inc.2023-05-22270
K220807Imperative Care Radial 088 Access SystemImperative Care, Inc.2022-05-17600
K212224TracStar LDP Large Distal Platform; Zoom 88 Large Distal PlaImperative Care, Inc.2021-09-20660
K211476ZOOM 71 Reperfusion Catheter; ZOOM Aspiration TubingImperative Care, Inc.2021-06-08270
K210996ZOOM (71, 55, 45, 35) Reperfusion Catheters; ZOOM AspirationImperative Care, Inc.2021-04-23211
K203764TracStar Large Distal Platform, ZOOM 88 Large Distal PlatforImperative Care, Inc.2021-03-03700
K202182ZOOM (71, 55, 45, 35) Reperfusion Catheters; ZOOM AspirationImperative Care, Inc.2020-09-02291
K1830430.071” ID MantaRay Reperfusion Catheter, 0.055” ID MantaRay Imperative Care, Inc.2019-04-171661
K180169EagleRay Long Sheath, 0.088 ID, 80cm, 90cm, 100cm and 110cm Imperative Care, Inc.2018-08-081980

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