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FDA 510(k)

Pump Alignment Syringe

K-Number: K220184 · 2022-07-21

ApplicantJiangsu Caina Medical Co.,Ltd
Decision Date2022-07-21
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Pump Alignment Syringe is a medical device manufactured by Jiangsu Caina Medical Co.,Ltd. It received FDA 510(k) clearance on 2022-07-21 under approval number K220184. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Pump Alignment Syringe?

Pump Alignment Syringe is a medical device that received FDA 510(k) clearance on 2022-07-21. It is manufactured by Jiangsu Caina Medical Co.,Ltd. The 510(k) number is K220184.

When was Pump Alignment Syringe approved by the FDA?

Pump Alignment Syringe received FDA 510(k) clearance on 2022-07-21, under approval number K220184.

What company makes Pump Alignment Syringe?

Pump Alignment Syringe is manufactured by Jiangsu Caina Medical Co.,Ltd.

What is the FDA product code for Pump Alignment Syringe?

The FDA product code for Pump Alignment Syringe is FMF.

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Related Devices (Code: FMF)

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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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