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FDA 510(k)

DISPENSING PIN WITH ONE-WAY VALVE

K-Number: K943181 · 1994-09-29

ApplicantB. Braun of America, Inc.
Decision Date1994-09-29
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPENSING PIN WITH ONE-WAY VALVE 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 1994-09-29 under 510(k) number K943181. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPENSING PIN WITH ONE-WAY VALVE?

DISPENSING PIN WITH ONE-WAY VALVE is a medical device that received FDA 510(k) clearance on 1994-09-29. The listed applicant is B. Braun of America, Inc.. The 510(k) number is K943181.

When did DISPENSING PIN WITH ONE-WAY VALVE receive FDA 510(k) clearance?

DISPENSING PIN WITH ONE-WAY VALVE received FDA 510(k) clearance on 1994-09-29, under 510(k) number K943181.

Who is the listed applicant for DISPENSING PIN WITH ONE-WAY VALVE?

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 DISPENSING PIN WITH ONE-WAY VALVE?

The FDA product code for DISPENSING PIN WITH ONE-WAY VALVE is LHI.

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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: LHI)

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.

K252987ADRx™ Admixture DeviceEpic Medical Pte. , Ltd.K260301Vial AdapterHangzhou Qiantang Longyue Biotechnology Co., Ltd.K250345Medline Bag DecanterMedline Industries, LPK251715FlowArt® Vial Access Device VentedAsset MedikalK251676Medline Microtek C-Flo Bag Decanter, Sterile (2000S); Medline Microtek Bag Decanter II, Sterile (2002S); Medline Microtek Vial Decanter, Sterile (2006S); Medline Microtek Transfer Device, Sterile (2008S)Microtek Medical, LLCK243404HyHub™ and HyHub™ Duo Vial Access DevicesTakeda Pharmaceuticals

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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