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FDA 510(k)

LOW VOLUME MULTIPORT

K-Number: K943770 · 1995-04-10

ApplicantB. Braun of America, Inc.
Decision Date1995-04-10
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LOW VOLUME MULTIPORT is the device name listed in this FDA 510(k) record. The listed applicant is B. Braun of America, Inc.. It received FDA 510(k) clearance on 1995-04-10 under 510(k) number K943770. 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 LOW VOLUME MULTIPORT?

LOW VOLUME MULTIPORT is a medical device that received FDA 510(k) clearance on 1995-04-10. The listed applicant is B. Braun of America, Inc.. The 510(k) number is K943770.

When did LOW VOLUME MULTIPORT receive FDA 510(k) clearance?

LOW VOLUME MULTIPORT received FDA 510(k) clearance on 1995-04-10, under 510(k) number K943770.

Who is the listed applicant for LOW VOLUME MULTIPORT?

The FDA 510(k) record lists B. Braun of America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOW VOLUME MULTIPORT?

The FDA product code for LOW VOLUME MULTIPORT is FPA.

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Other records listing B. Braun of America, Inc. 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.

K993024CELSITE IMPLANTABLE PORT WITH VALVED CATHETERK983794CHEMO MINI SPIKE PLUSK946170COMFORT-Q SUBCUTANEOUS INJECTION SETSK945850BRAUN DIACAN(R) FISTULA NEEDLESK942988FILTERED EXTENSION SETSK945752CELSITE(TM) BRACHIAL VENOUS PORT

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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

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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