Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

VERSA-LOCK(TM) UNIVERSAL NEEDLE CONNECTOR

K-Number: K901046 · 1990-06-08

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

Device Summary

VERSA-LOCK(TM) UNIVERSAL NEEDLE CONNECTOR 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 K901046. 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 VERSA-LOCK(TM) UNIVERSAL NEEDLE CONNECTOR?

VERSA-LOCK(TM) UNIVERSAL NEEDLE CONNECTOR 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 K901046.

When did VERSA-LOCK(TM) UNIVERSAL NEEDLE CONNECTOR receive FDA 510(k) clearance?

VERSA-LOCK(TM) UNIVERSAL NEEDLE CONNECTOR received FDA 510(k) clearance on 1990-06-08, under 510(k) number K901046.

Who is the listed applicant for VERSA-LOCK(TM) UNIVERSAL NEEDLE CONNECTOR?

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 VERSA-LOCK(TM) UNIVERSAL NEEDLE CONNECTOR?

The FDA product code for VERSA-LOCK(TM) UNIVERSAL NEEDLE CONNECTOR 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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

View all 12 devices →

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.

↑