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

ShockPulse-SE Lithotripsy System

K Number: K171024 · Decision Aug 21, 2017
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
13
Applicant Total
7
Review Days
138

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Basic Information

Device Name
ShockPulse-SE Lithotripsy System
K Number
K171024
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4480
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cybersonics, Inc.
Date Received
April 5, 2017
Decision Date
August 21, 2017
Product Code
FEO
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FEO Lithotriptor, Ultrasonic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FEO), ordered by most recent decision date.

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Other Clearances by Cybersonics, Inc.

K Number Device Name
K142428 Shock Pulse-SE Lithotripsy System CYBERWAND II
K132795 CYBERWAND STERILE PROBE SET
K120303 CYBERWAND DUAL ACTION ULTRASONIC LITHOTRIPSY SYSTEM
K102169 CYBERWAND LITHOTRIPTER
K072422 CYBERWAND STERILE PADS, MODEL: CW-RBPBX
K052135 CYBERSONICS CYBERWAND DUAL PROBE LITHOTRIPTER