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

URO PRO

K Number: K042457 · Decision Oct 25, 2004
Classifications
1
FEI Numbers
76
Registration Numbers
76
Same Product Code
27
Applicant Total
15
Review Days
45

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Basic Information

Device Name
URO PRO
K Number
K042457
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
W.O.M. World of Medicine AG
Date Received
September 10, 2004
Decision Date
October 25, 2004
Product Code
LJH
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
LJH System, Irrigation, Urological

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Other Clearances by W.O.M. World of Medicine AG

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K062380 FLOSIMPLE ARTHROSCOPY PUMP A120
K060723 40 L HIGH FLOW INSUFFLATOR F113
K030837 40 L HIGH FLOW INSUFFLATOR F108
K033927 ARTHOSCOPY PUMP A115
K032023 W.O.M. LASER U100PLUS
K022721 UROPOWER
K031616 IUR FLUID MANAGEMENT SYSTEM
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