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

SYSTEM 1E LIQUID CHEMICAL STERILANT PROCESSING SYSTEM

K Number: K102462 · Decision Sep 21, 2010
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
62
Applicant Total
169
Review Days
25

Basic Information

Device Name
SYSTEM 1E LIQUID CHEMICAL STERILANT PROCESSING SYSTEM
K Number
K102462
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.6885
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
STERIS Corporation
Date Received
August 27, 2010
Decision Date
September 21, 2010
Product Code
MED
Advisory Committee
General Hospital
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
MED Sterilant, Medical Devices

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