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

CPS Locator 3D Plus Delivery Catheter

K Number: K250828 · Decision Jun 27, 2025
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
13
Review Days
100

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Basic Information

Device Name
CPS Locator 3D Plus Delivery Catheter
K Number
K250828
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CenterPoint Systems, LLC
Date Received
March 19, 2025
Decision Date
June 27, 2025
Product Code
DQY
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DQY Catheter, Percutaneous

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K Number Device Name
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K251051 AuST Steerable Sheath
K243180 SSPC NXT Delivery Catheter
K242106 AuST Steerable Sheath
K233752 Dragonfly™ Pancreaticobiliary Scope; Dragonfly™ Digital Controller; Dragonfly™ Instrument Channel Caps
K240829 AuST Steerable Sheath
K223097 RenaNav Ureteroscope System
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