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)

PERIPHERAL INTERVENOUS CATHETER

K-Number: K914378 · 1993-05-20

ApplicantMedical Profiles, Inc.
Decision Date1993-05-20
Product CodeFOZ
Advisory CommitteeHO
DecisionUnknown

Device Summary

PERIPHERAL INTERVENOUS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Profiles, Inc.. It received FDA 510(k) clearance on 1993-05-20 under 510(k) number K914378. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the PERIPHERAL INTERVENOUS CATHETER?

PERIPHERAL INTERVENOUS CATHETER is a medical device that received FDA 510(k) clearance on 1993-05-20. The listed applicant is Medical Profiles, Inc.. The 510(k) number is K914378.

When did PERIPHERAL INTERVENOUS CATHETER receive FDA 510(k) clearance?

PERIPHERAL INTERVENOUS CATHETER received FDA 510(k) clearance on 1993-05-20, under 510(k) number K914378.

Who is the listed applicant for PERIPHERAL INTERVENOUS CATHETER?

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

What is the FDA product code for PERIPHERAL INTERVENOUS CATHETER?

The FDA product code for PERIPHERAL INTERVENOUS CATHETER is FOZ.

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 Medical Profiles, 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.

K884327EXCEL Y-CONNECTOR CAT. #E-201K883769EXCEL INFLATE-AID

Related Devices (Code: FOZ)

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.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, Inc.

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.

↑