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FDA 510(k)

Celerity 20 HP Biological Indicator

K-Number: K172474 · 2017-12-29

Decision Date2017-12-29
Product CodeFRC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Celerity 20 HP Biological Indicator is a medical device manufactured by STERIS Corporation. It received FDA 510(k) clearance on 2017-12-29 under approval number K172474. The device is classified under product code FRC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Celerity 20 HP Biological Indicator?

Celerity 20 HP Biological Indicator is a medical device that received FDA 510(k) clearance on 2017-12-29. It is manufactured by STERIS Corporation. The 510(k) number is K172474.

When was Celerity 20 HP Biological Indicator approved by the FDA?

Celerity 20 HP Biological Indicator received FDA 510(k) clearance on 2017-12-29, under approval number K172474.

What company makes Celerity 20 HP Biological Indicator?

Celerity 20 HP Biological Indicator is manufactured by STERIS Corporation.

What is the FDA product code for Celerity 20 HP Biological Indicator?

The FDA product code for Celerity 20 HP Biological Indicator is FRC.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.