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)

MPS ACACIA SAFEGUARD HUBER DEVICE

K-Number: K032934 · 2003-11-13

ApplicantMps Acacia
Decision Date2003-11-13
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MPS ACACIA SAFEGUARD HUBER DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Mps Acacia. It received FDA 510(k) clearance on 2003-11-13 under 510(k) number K032934. 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 MPS ACACIA SAFEGUARD HUBER DEVICE?

MPS ACACIA SAFEGUARD HUBER DEVICE is a medical device that received FDA 510(k) clearance on 2003-11-13. The listed applicant is Mps Acacia. The 510(k) number is K032934.

When did MPS ACACIA SAFEGUARD HUBER DEVICE receive FDA 510(k) clearance?

MPS ACACIA SAFEGUARD HUBER DEVICE received FDA 510(k) clearance on 2003-11-13, under 510(k) number K032934.

Who is the listed applicant for MPS ACACIA SAFEGUARD HUBER DEVICE?

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

What is the FDA product code for MPS ACACIA SAFEGUARD HUBER DEVICE?

The FDA product code for MPS ACACIA SAFEGUARD HUBER DEVICE 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 Mps Acacia 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.

K090809MPS ACACIA POWER INJECTABLE INFUSION SETK080328MPS ACACIA ENTERAL FEEDING TUBEK052451MPS ACACIA MEDFLO ELASTOMERIC PUMPK052946MPS ACACIA NERVE BLOCK NEEDLEK011117MPS ACACIA MEDFLO INFUSION (LI) AND MPS ACACIA MEDFLO INFUSION (LI) KEEP VEIN OPEN (KVO) ELASTOMERIC PUMPSK003476MPS ACACIA PAIN KIT

View all 7 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.

↑