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FDA 510(k)

Safety Sliding Blood Collection Set

K-Number: K232781 · 2024-03-07

ApplicantJiangsu Caina Medical Co.,Ltd
Decision Date2024-03-07
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

Safety Sliding Blood Collection Set is a medical device manufactured by Jiangsu Caina Medical Co.,Ltd. It received FDA 510(k) clearance on 2024-03-07 under approval number K232781. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Safety Sliding Blood Collection Set?

Safety Sliding Blood Collection Set is a medical device that received FDA 510(k) clearance on 2024-03-07. It is manufactured by Jiangsu Caina Medical Co.,Ltd. The 510(k) number is K232781.

When was Safety Sliding Blood Collection Set approved by the FDA?

Safety Sliding Blood Collection Set received FDA 510(k) clearance on 2024-03-07, under approval number K232781.

What company makes Safety Sliding Blood Collection Set?

Safety Sliding Blood Collection Set is manufactured by Jiangsu Caina Medical Co.,Ltd.

What is the FDA product code for Safety Sliding Blood Collection Set?

The FDA product code for Safety Sliding Blood Collection Set is JKA.

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Related PubMed Literature

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Other Devices by Jiangsu Caina Medical Co.,Ltd

K181374NRFit Syringe K172938Disposable Sterile Needle K191490Retractable Safety Syringe, Retractable Safety Insulin Syringe, Retractable Safety Tuberculin Syringe, Retractable Safety Allergy Syringe K190502ENFit Oral / Enteral Syringe K200027Blood Collection Needle with/without Holder, Safety Blood Collection Needle with/without Holder, Luer Access Device-holder with Preattached Multiple Sample Adapter K193022Retractable Safety Insulin Syringe

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Related Devices (Code: JKA)

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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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