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FDA 510(k)

VLV SA EF INFUSION PORT

K-Number: K953791 · 1995-10-30

ApplicantVlv Associates, Inc.
Decision Date1995-10-30
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VLV SA EF INFUSION PORT is the device name listed in this FDA 510(k) record. The listed applicant is Vlv Associates, Inc.. It received FDA 510(k) clearance on 1995-10-30 under 510(k) number K953791. 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 VLV SA EF INFUSION PORT?

VLV SA EF INFUSION PORT is a medical device that received FDA 510(k) clearance on 1995-10-30. The listed applicant is Vlv Associates, Inc.. The 510(k) number is K953791.

When did VLV SA EF INFUSION PORT receive FDA 510(k) clearance?

VLV SA EF INFUSION PORT received FDA 510(k) clearance on 1995-10-30, under 510(k) number K953791.

Who is the listed applicant for VLV SA EF INFUSION PORT?

The FDA 510(k) record lists Vlv Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VLV SA EF INFUSION PORT?

The FDA product code for VLV SA EF INFUSION PORT is FPA.

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Other records listing Vlv Associates, 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.

K972957SA-EF MULTI-LUMEN EXTENSION SETK964876SA.EF(TM) INFUSION PORT II - CONNECTOR AND EXTENSION SETK955783VLV SA.EF INFUSION PORT EXTENSION SETSK945592VLV SOLODRAW(TM) DUAL CHAMBER PISTON SYRINGEK940406DISPOSABLE, AMBULATORY, INFUSION PUMPSK933364PROMED BIOPSY NEEDLE

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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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