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

STRYKER URETEROSCOPE

K Number: K043021 · Decision Mar 16, 2005
Classifications
1
FEI Numbers
120
Registration Numbers
120
Same Product Code
112
Applicant Total
101
Review Days
133

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Basic Information

Device Name
STRYKER URETEROSCOPE
K Number
K043021
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Endoscopy
Date Received
November 3, 2004
Decision Date
March 16, 2005
Product Code
FGB
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
FGB Ureteroscope And Accessories, Flexible/Rigid

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