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FDA 510(k)

FREE FLOW SAFETY DEVICE, MODEL MG 245052

K-Number: K990288 · 1999-02-24

ApplicantTeva Medical, Ltd.
Decision Date1999-02-24
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FREE FLOW SAFETY DEVICE, MODEL MG 245052 is the device name listed in this FDA 510(k) record. The listed applicant is Teva Medical, Ltd.. It received FDA 510(k) clearance on 1999-02-24 under 510(k) number K990288. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FREE FLOW SAFETY DEVICE, MODEL MG 245052?

FREE FLOW SAFETY DEVICE, MODEL MG 245052 is a medical device that received FDA 510(k) clearance on 1999-02-24. The listed applicant is Teva Medical, Ltd.. The 510(k) number is K990288.

When did FREE FLOW SAFETY DEVICE, MODEL MG 245052 receive FDA 510(k) clearance?

FREE FLOW SAFETY DEVICE, MODEL MG 245052 received FDA 510(k) clearance on 1999-02-24, under 510(k) number K990288.

Who is the listed applicant for FREE FLOW SAFETY DEVICE, MODEL MG 245052?

The FDA 510(k) record lists Teva Medical, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FREE FLOW SAFETY DEVICE, MODEL MG 245052?

The FDA product code for FREE FLOW SAFETY DEVICE, MODEL MG 245052 is FPA.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Teva Medical, Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: FPA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K254123Ecomed Disposable Administration SetsEcomed Solutions, LLCK261530iiSure Infusion SetDeka Research and DevelopmentK252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)Amsino International, Inc.K251375PuraCath Firefly Needleless Connector IT (9005)Puracath Medical, Inc.K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]Np MedicalK250325BD Alaris Pump Infusion SetCarefusion (Bd)

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.

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