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

MODULAR DISINFECTION SYSTEM (MDS) FOR ENDOSCOPE REPROCESSING

K Number: K063876 · Decision Jun 14, 2007
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
56
Applicant Total
3
Review Days
167

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Basic Information

Device Name
MODULAR DISINFECTION SYSTEM (MDS) FOR ENDOSCOPE REPROCESSING
K Number
K063876
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medivators Reprocessing Systems
Date Received
December 29, 2006
Decision Date
June 14, 2007
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FEB), ordered by most recent decision date.

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Other Clearances by Medivators Reprocessing Systems

K Number Device Name
K102996 MEDIVATORS ADVANTAGE PLUS ENDOSCOPE REPROCESSOR
K082988 MEDIVATORS ADVANTAGE PLUS ENDOSCOPE REPROCESSING SYSTEM, RAPICIDE PA HIGH LEVEL DISINFECTANT