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

System 83 Revolve Endoscope Washer/Disinfector

K Number: K241168 · Decision Dec 19, 2024
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
57
Applicant Total
1
Review Days
237

Basic Information

Device Name
System 83 Revolve Endoscope Washer/Disinfector
K Number
K241168
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Wassenburg Medical, Inc.
Date Received
April 26, 2024
Decision Date
December 19, 2024
Product Code
FEB
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FEB Accessories, Cleaning, For Endoscope

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