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

SYSTEM 1E Liquid Chemical Sterilant Processing System, Model P6700; SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900

K Number: K251666 · Decision Apr 8, 2026
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
63
Applicant Total
204
Review Days
313

Basic Information

Device Name
SYSTEM 1E Liquid Chemical Sterilant Processing System, Model P6700; SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900
K Number
K251666
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6885
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
STERIS Corporation
Date Received
May 30, 2025
Decision Date
April 8, 2026
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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