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FDA 510(k)

OK Plus Indicator

K-Number: K222137 · 2022-12-05

ApplicantPropper Manufacturing Co., Inc.
Decision Date2022-12-05
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OK Plus Indicator is a medical device manufactured by Propper Manufacturing Co., Inc.. It received FDA 510(k) clearance on 2022-12-05 under approval number K222137. 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 OK Plus Indicator?

OK Plus Indicator is a medical device that received FDA 510(k) clearance on 2022-12-05. It is manufactured by Propper Manufacturing Co., Inc.. The 510(k) number is K222137.

When was OK Plus Indicator approved by the FDA?

OK Plus Indicator received FDA 510(k) clearance on 2022-12-05, under approval number K222137.

What company makes OK Plus Indicator?

OK Plus Indicator is manufactured by Propper Manufacturing Co., Inc..

What is the FDA product code for OK Plus Indicator?

The FDA product code for OK Plus Indicator is JOJ.

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Related Devices (Code: 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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