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FDA 510(k)

Celerity Chemical Indicator for enspire 3000 CLCSPS

K-Number: K240032 · 2024-04-17

Decision Date2024-04-17
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Celerity Chemical Indicator for enspire 3000 CLCSPS is a medical device manufactured by STERIS Corporation. It received FDA 510(k) clearance on 2024-04-17 under approval number K240032. 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 Chemical Indicator for enspire 3000 CLCSPS?

Celerity Chemical Indicator for enspire 3000 CLCSPS is a medical device that received FDA 510(k) clearance on 2024-04-17. It is manufactured by STERIS Corporation. The 510(k) number is K240032.

When was Celerity Chemical Indicator for enspire 3000 CLCSPS approved by the FDA?

Celerity Chemical Indicator for enspire 3000 CLCSPS received FDA 510(k) clearance on 2024-04-17, under approval number K240032.

What company makes Celerity Chemical Indicator for enspire 3000 CLCSPS?

Celerity Chemical Indicator for enspire 3000 CLCSPS is manufactured by STERIS Corporation.

What is the FDA product code for Celerity Chemical Indicator for enspire 3000 CLCSPS?

The FDA product code for Celerity Chemical Indicator for enspire 3000 CLCSPS is JOJ.

Other Devices by STERIS Corporation

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Related Devices (Code: JOJ)

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.