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FDA 510(k)

BD Plastipak Syringe

K-Number: K182589 · 2019-03-14

ApplicantBecton, Dickinson and Company
Decision Date2019-03-14
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BD Plastipak Syringe is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2019-03-14 under approval number K182589. 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 BD Plastipak Syringe?

BD Plastipak Syringe is a medical device that received FDA 510(k) clearance on 2019-03-14. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K182589.

When was BD Plastipak Syringe approved by the FDA?

BD Plastipak Syringe received FDA 510(k) clearance on 2019-03-14, under approval number K182589.

What company makes BD Plastipak Syringe?

BD Plastipak Syringe is manufactured by Becton, Dickinson and Company.

What is the FDA product code for BD Plastipak Syringe?

The FDA product code for BD Plastipak Syringe is FMF.

Other Devices by Becton, Dickinson and Company

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Related Devices (Code: FMF)

K162180Disposable Insulin SyringeBerpu Medical Technology Co., Ltd. K162081BD 1ml Luer-lok Hypodermic Syringe, BD 1 mL Luer-Lok Hypodermic Syringe with BD Hypodermic Needle or BD Eclipse Hypodermic Needle, BD 1ml Luer-lok Insulin SyringeBecton, Dickinson and Company K162602NovoPen EchoNovo Nordisk, Inc. K161568Bone Solutions Mixing and Delivery SystemBone Solutions, Inc. K152879Sure-Fine Insulin SyringesShina Med Corporation K160629InPenCompanion Medical, Inc.

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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