AMSCO 700 Steam Sterilizer

FDA 510(k) K261055 · STERIS Corporation

Substantially Equivalent

510(k) numberK261055

Submission

Device name
AMSCO 700 Steam Sterilizer
Applicant
STERIS Corporation
Mentor, OH, US
Received
March 31, 2026
Decision date
June 24, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FLE – Sterilizer, Steam
Device class
Class II (moderate risk)
Regulation
21 CFR 880.6880
Specialty
General Hospital

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Questions and answers

When was AMSCO 700 Steam Sterilizer cleared by the FDA?

AMSCO 700 Steam Sterilizer (K261055) received a 510(k) decision of Substantially Equivalent on June 24, 2026, 85 days after the submission was received.

What is the product code of K261055?

The FDA product code is FLE – Sterilizer, Steam, a Class II (moderate risk) device regulated under 21 CFR 880.6880.