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FDA 510(k)

VICTUS I.V. ADMINISTRATION SET, MODELS 27058, 27059,27062

K-Number: K023469 · 2002-12-10

ApplicantVictus, Inc.
Decision Date2002-12-10
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VICTUS I.V. ADMINISTRATION SET, MODELS 27058, 27059,27062 is the device name listed in this FDA 510(k) record. The listed applicant is Victus, Inc.. It received FDA 510(k) clearance on 2002-12-10 under 510(k) number K023469. 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 VICTUS I.V. ADMINISTRATION SET, MODELS 27058, 27059,27062?

VICTUS I.V. ADMINISTRATION SET, MODELS 27058, 27059,27062 is a medical device that received FDA 510(k) clearance on 2002-12-10. The listed applicant is Victus, Inc.. The 510(k) number is K023469.

When did VICTUS I.V. ADMINISTRATION SET, MODELS 27058, 27059,27062 receive FDA 510(k) clearance?

VICTUS I.V. ADMINISTRATION SET, MODELS 27058, 27059,27062 received FDA 510(k) clearance on 2002-12-10, under 510(k) number K023469.

Who is the listed applicant for VICTUS I.V. ADMINISTRATION SET, MODELS 27058, 27059,27062?

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

What is the FDA product code for VICTUS I.V. ADMINISTRATION SET, MODELS 27058, 27059,27062?

The FDA product code for VICTUS I.V. ADMINISTRATION SET, MODELS 27058, 27059,27062 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 Victus, 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.

K093271EXTENSION SET (STANDARDBORE TUBING), EXTENSION SET (MINIBORE TUBING), IV ADMINISTRATION SET ( STANDARDK030246VICTUS I.V. ADMINISTRATION SET, MODELS 27071 AND 27072

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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