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)

MODEL D-285N ADMINISTRATION SET

K-Number: K954841 · 1995-12-11

ApplicantPatient Solutions, Inc.
Decision Date1995-12-11
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL D-285N ADMINISTRATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Patient Solutions, Inc.. It received FDA 510(k) clearance on 1995-12-11 under 510(k) number K954841. 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 MODEL D-285N ADMINISTRATION SET?

MODEL D-285N ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1995-12-11. The listed applicant is Patient Solutions, Inc.. The 510(k) number is K954841.

When did MODEL D-285N ADMINISTRATION SET receive FDA 510(k) clearance?

MODEL D-285N ADMINISTRATION SET received FDA 510(k) clearance on 1995-12-11, under 510(k) number K954841.

Who is the listed applicant for MODEL D-285N ADMINISTRATION SET?

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

What is the FDA product code for MODEL D-285N ADMINISTRATION SET?

The FDA product code for MODEL D-285N ADMINISTRATION SET 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 Patient Solutions, 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.

K964384MODEL D-290P ADMINISTRATION SETK961263MODEL 1200 ABMULATORY INFUSION PUMPK953270MODEL 1100 MEDMATE INFUSION PUMPK894028AMBULATORY INFUSION SYSTEM AND ACCESSORIES

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.

↑