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FDA 510(k)

PHOENIX 5 URODYNAMICS SYSTEM

K-Number: K914300 · 1992-06-02

ApplicantAspen Medical , Ltd.
Decision Date1992-06-02
Product CodeFAP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PHOENIX 5 URODYNAMICS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Aspen Medical , Ltd.. It received FDA 510(k) clearance on 1992-06-02 under 510(k) number K914300. The device is classified under product code FAP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOENIX 5 URODYNAMICS SYSTEM?

PHOENIX 5 URODYNAMICS SYSTEM is a medical device that received FDA 510(k) clearance on 1992-06-02. The listed applicant is Aspen Medical , Ltd.. The 510(k) number is K914300.

When did PHOENIX 5 URODYNAMICS SYSTEM receive FDA 510(k) clearance?

PHOENIX 5 URODYNAMICS SYSTEM received FDA 510(k) clearance on 1992-06-02, under 510(k) number K914300.

Who is the listed applicant for PHOENIX 5 URODYNAMICS SYSTEM?

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

What is the FDA product code for PHOENIX 5 URODYNAMICS SYSTEM?

The FDA product code for PHOENIX 5 URODYNAMICS SYSTEM is FAP.

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

Related Devices (Code: FAP)

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.

K113771SIGNAL GEAR URETHRAL CATHETER ELECTRODENeurovision Medical Products, Inc.K974775SINGLE CHANNEL UROLOGICAL PRESSURE GAUGE, DUAL CHANNEL UROLOGICAL PRESSURE GAUGEAirtronic Services, Inc.K963330URODYNAMIC ANALYSIS MODULESynectics Medical, Inc.K962472RUSCH URODYNAMIC RECTAL BALLOON 2-WAY CATHETERRusch Intl.K931175SCHUSTER DISPOSABLE BALLOON PROBESandhill Scientific, Inc.K931179UROLAB SPECTRUMLife-Tech Intl., Inc.

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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