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

ViperCath XC Peripheral Exchange Catheter

K Number: K183000 · Decision Dec 29, 2018
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
26
Review Days
60

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Basic Information

Device Name
ViperCath XC Peripheral Exchange Catheter
K Number
K183000
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cardiovascular Systems, Inc.
Date Received
October 30, 2018
Decision Date
December 29, 2018
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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Other Clearances by Cardiovascular Systems, Inc.

K Number Device Name
K220109 DIAMONDBACK 360 Peripheral Orbital Atherectomy System, DIAMONDBACK 360 Peripheral Orbital Atherectomy System, Exchangeable Series, Stealth 360 Peripheral Orbital Atherectomy System
K212725 ViperCross Support Catheters
K210586 Diamonback 360 Peripheral Orbital Atherectomy System, Diamondback 360 Stealth Orbital Atherectomy system
K211240 ViperCross Support Catheters
K211251 ViperCath XC Peripheral Exchange Catheter
K210282 WIRION Embolic Protection System
K203008 DIAMONDBACK 360 Peripheral Orbital Atherectomy System, DIAMONDBACK 360 Peripheral Orbital Atherectomy System, Exchangeable Series, Stealth 360 Peripheral Orbital Atherectomy System
K200198 WIRION
K190634 Diamondback 360 Peripheral Orbital Atherectomy System, Stealth 360 Peripheral Orbital Atherectomy System
K182397 Diamondback 360 Peripheral Orbital Atherectomy System Exchangeable Series
Search all 26 clearances from Cardiovascular Systems, Inc. →