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FDA 510(k)

Celerity HP Chemical Indicator (CI)

K-Number: K183295 · 2019-01-04

ApplicantSteris Corporations
Decision Date2019-01-04
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Celerity HP Chemical Indicator (CI) is a medical device manufactured by Steris Corporations. It received FDA 510(k) clearance on 2019-01-04 under approval number K183295. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Celerity HP Chemical Indicator (CI)?

Celerity HP Chemical Indicator (CI) is a medical device that received FDA 510(k) clearance on 2019-01-04. It is manufactured by Steris Corporations. The 510(k) number is K183295.

When was Celerity HP Chemical Indicator (CI) approved by the FDA?

Celerity HP Chemical Indicator (CI) received FDA 510(k) clearance on 2019-01-04, under approval number K183295.

What company makes Celerity HP Chemical Indicator (CI)?

Celerity HP Chemical Indicator (CI) is manufactured by Steris Corporations.

What is the FDA product code for Celerity HP Chemical Indicator (CI)?

The FDA product code for Celerity HP Chemical Indicator (CI) is JOJ.

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Official Source

View on FDA Database →

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

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