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)

BJ STAR ALL SILICONE FOLEY BALLOON CATHETER

K-Number: K900022 · 1990-03-15

ApplicantB.J. Star, Inc.
Decision Date1990-03-15
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BJ STAR ALL SILICONE FOLEY BALLOON CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is B.J. Star, Inc.. It received FDA 510(k) clearance on 1990-03-15 under 510(k) number K900022. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BJ STAR ALL SILICONE FOLEY BALLOON CATHETER?

BJ STAR ALL SILICONE FOLEY BALLOON CATHETER is a medical device that received FDA 510(k) clearance on 1990-03-15. The listed applicant is B.J. Star, Inc.. The 510(k) number is K900022.

When did BJ STAR ALL SILICONE FOLEY BALLOON CATHETER receive FDA 510(k) clearance?

BJ STAR ALL SILICONE FOLEY BALLOON CATHETER received FDA 510(k) clearance on 1990-03-15, under 510(k) number K900022.

Who is the listed applicant for BJ STAR ALL SILICONE FOLEY BALLOON CATHETER?

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

What is the FDA product code for BJ STAR ALL SILICONE FOLEY BALLOON CATHETER?

The FDA product code for BJ STAR ALL SILICONE FOLEY BALLOON CATHETER is KOD.

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: KOD)

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.

K251864Rubber Utility CatheterC.R. Bard, Inc.K220036Wellead Ureteral CatheterWell Lead Medical Co., Ltd.K220730allFlex Ureteral Catheters, Krait Ureteral CathetersAllwin Medical Devices, Inc.K211032Urinary Catheter 12 Fr, Urinary Catheter 16 FrUrogen Pharma, Ltd.K181979Rusch FloCath Quick 18 Fr. Coudé Hydrophilic Intermittent CatheterTeleflexmedical, Inc.K180354UroGen Ureteral CatheterUrogen Pharma, Ltd.

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.

↑