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

ACMI AUTOCLAVABLE URETEROSCOPE, MODELS MR-6A AND MR-6AL

K Number: K052044 · Decision Aug 16, 2005
Classifications
1
FEI Numbers
109
Registration Numbers
109
Same Product Code
103
Applicant Total
16
Review Days
19

Basic Information

Device Name
ACMI AUTOCLAVABLE URETEROSCOPE, MODELS MR-6A AND MR-6AL
K Number
K052044
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ACMI CORPORATION
Date Received
July 28, 2005
Decision Date
August 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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