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FDA 510(k)

PRO-LOCK(TM) SHIELDING NEEDLE CONNECTOR ASSEMBLY

K-Number: K901081 · 1990-06-08

ApplicantVlv Associates, Inc.
Decision Date1990-06-08
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PRO-LOCK(TM) SHIELDING NEEDLE CONNECTOR ASSEMBLY 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 1990-06-08 under 510(k) number K901081. 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 PRO-LOCK(TM) SHIELDING NEEDLE CONNECTOR ASSEMBLY?

PRO-LOCK(TM) SHIELDING NEEDLE CONNECTOR ASSEMBLY is a medical device that received FDA 510(k) clearance on 1990-06-08. The listed applicant is Vlv Associates, Inc.. The 510(k) number is K901081.

When did PRO-LOCK(TM) SHIELDING NEEDLE CONNECTOR ASSEMBLY receive FDA 510(k) clearance?

PRO-LOCK(TM) SHIELDING NEEDLE CONNECTOR ASSEMBLY received FDA 510(k) clearance on 1990-06-08, under 510(k) number K901081.

Who is the listed applicant for PRO-LOCK(TM) SHIELDING NEEDLE CONNECTOR ASSEMBLY?

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 PRO-LOCK(TM) SHIELDING NEEDLE CONNECTOR ASSEMBLY?

The FDA product code for PRO-LOCK(TM) SHIELDING NEEDLE CONNECTOR ASSEMBLY 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 SETSK953791VLV SA EF INFUSION PORTK945592VLV SOLODRAW(TM) DUAL CHAMBER PISTON SYRINGEK940406DISPOSABLE, AMBULATORY, INFUSION PUMPS

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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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