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FDA 510(k)

DOSI-FLOW, MODELS 20 & 30

K-Number: K952810 · 1995-09-08

ApplicantLeventon, S.A.
Decision Date1995-09-08
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DOSI-FLOW, MODELS 20 & 30 is the device name listed in this FDA 510(k) record. The listed applicant is Leventon, S.A.. It received FDA 510(k) clearance on 1995-09-08 under 510(k) number K952810. 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 DOSI-FLOW, MODELS 20 & 30?

DOSI-FLOW, MODELS 20 & 30 is a medical device that received FDA 510(k) clearance on 1995-09-08. The listed applicant is Leventon, S.A.. The 510(k) number is K952810.

When did DOSI-FLOW, MODELS 20 & 30 receive FDA 510(k) clearance?

DOSI-FLOW, MODELS 20 & 30 received FDA 510(k) clearance on 1995-09-08, under 510(k) number K952810.

Who is the listed applicant for DOSI-FLOW, MODELS 20 & 30?

The FDA 510(k) record lists Leventon, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DOSI-FLOW, MODELS 20 & 30?

The FDA product code for DOSI-FLOW, MODELS 20 & 30 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 Leventon, S.A. 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.

K053149SPIRO-BALLK040752DOSI-FUSERK994074TRI-BALLK851058DOSI FLOW

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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