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

MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM

K Number: K092387 · Decision Apr 5, 2010
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
56
Applicant Total
33
Review Days
243

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Basic Information

Device Name
MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM
K Number
K092387
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Minntech Corp.
Date Received
August 5, 2009
Decision Date
April 5, 2010
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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