FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Zoom System (Zoom 4S Catheter)

K Number: K252046 · Decision Oct 30, 2025
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
108
Applicant Total
17
Review Days
122

Basic Information

Device Name
Zoom System (Zoom 4S Catheter)
K Number
K252046
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Imperative Care, Inc.
Date Received
June 30, 2025
Decision Date
October 30, 2025
Product Code
NRY
Advisory Committee
Cardiovascular
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NRY Catheter, Thrombus Retriever

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Other Clearances by Imperative Care, Inc.

K Number Device Name
K252057 Symphony™ Thrombectomy System and Symphony™ 16F 82cm Thrombectomy System
K244061 X-Wire Guidewire
K243047 Zoom 7X Catheter; Zoom Aspiration Tubing; Zoom POD Aspiration Tubing
K250775 Symphony™ Thrombectomy System; Symphony™ 16F 82cm Thrombectomy System
K242672 Zoom System
K240948 TracStar LDP Large Distal Platform; Zoom 88 Large Distal Platform; Zoom 88 Large Distal Platform Support
K233975 Zoom 6F Insert Catheters
K231168 TracStar LDP Large Distal Platform; Zoom 88 Large Distal Platform; Zoom 88 Large Distal Platform Support
K220807 Imperative Care Radial 088 Access System
K212224 TracStar LDP Large Distal Platform; Zoom 88 Large Distal Platform
Search all 17 clearances from Imperative Care, Inc. →