gke Steri-Record Steam Mini-Bio-Plus self-contained biological indicator (SCBI)

FDA 510(k) K163144 · Gke-GmbH

Substantially Equivalent

510(k) numberK163144

Submission

Device name
gke Steri-Record Steam Mini-Bio-Plus self-contained biological indicator (SCBI)
Applicant
Gke-GmbH
Waldems, DE
Received
November 9, 2016
Decision date
April 7, 2017
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FRC – Indicator, Biological Sterilization Process
Device class
Class II (moderate risk)
Regulation
21 CFR 880.2800
Specialty
General Hospital

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Questions and answers

When was gke Steri-Record Steam Mini-Bio-Plus self-contained biological indicator (SCBI) cleared by the FDA?

gke Steri-Record Steam Mini-Bio-Plus self-contained biological indicator (SCBI) (K163144) received a 510(k) decision of Substantially Equivalent on April 7, 2017, 149 days after the submission was received.

What is the product code of K163144?

The FDA product code is FRC – Indicator, Biological Sterilization Process, a Class II (moderate risk) device regulated under 21 CFR 880.2800.