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

EOGas 4 Endo-SteriTest RRBI

K Number: K202879 · Decision Mar 3, 2021
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
205
Applicant Total
19
Review Days
156

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Basic Information

Device Name
EOGas 4 Endo-SteriTest RRBI
K Number
K202879
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2800
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Andersen Sterilizers, Inc.
Date Received
September 28, 2020
Decision Date
March 3, 2021
Product Code
FRC
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
FRC Indicator, Biological Sterilization Process

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Other Clearances by Andersen Sterilizers, Inc.

K Number Device Name
K213296 Anprolene SteriTest RRBI
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K200335 Sterisheet Sterilization Wrap
K192978 EOGas 4 Ethylene Oxide Gas Sterilizer
K192980 EOGas 4 Endo-SteriTest
K200336 Tyvek Sterilization Pouches with Chevron Seal
K170437 Sterisheet Sterilization Wrap
K170439 AN87 Dosimeter
K170432 Anprolene AN75 Ethylene Oxide Gas Sterilizer
K170427 Anprolene SteriTest
Search all 19 clearances from Andersen Sterilizers, Inc. →