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)

WILSON-COOK BALLOON DILATION CATHETERS

K-Number: K900924 · 1990-12-21

ApplicantWilson-Cook Medical, Inc.
Decision Date1990-12-21
Product CodeKNQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WILSON-COOK BALLOON DILATION CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Wilson-Cook Medical, Inc.. It received FDA 510(k) clearance on 1990-12-21 under 510(k) number K900924. The device is classified under product code KNQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILSON-COOK BALLOON DILATION CATHETERS?

WILSON-COOK BALLOON DILATION CATHETERS is a medical device that received FDA 510(k) clearance on 1990-12-21. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K900924.

When did WILSON-COOK BALLOON DILATION CATHETERS receive FDA 510(k) clearance?

WILSON-COOK BALLOON DILATION CATHETERS received FDA 510(k) clearance on 1990-12-21, under 510(k) number K900924.

Who is the listed applicant for WILSON-COOK BALLOON DILATION CATHETERS?

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

What is the FDA product code for WILSON-COOK BALLOON DILATION CATHETERS?

The FDA product code for WILSON-COOK BALLOON DILATION CATHETERS is KNQ.

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 Wilson-Cook Medical, 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.

K253302Hemospray Endoscopic Hemostat (HEMO-[X])K243568Teslatome Bipolar Sphincterotome; Tesla BiCord Active CordK213356Entuit PEG, Entuit PEGJK212323Instinct Plus Endoscopic Clipping DeviceK201322Entuit Nasal Jejunal Feeding TubeK200972Hemospray Endoscopic Hemostat

View all 122 devices →

Related Devices (Code: KNQ)

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.

K122924CRE FIXED WIRE BALLON DILATION CATHETERBoston Scientific CorpK093236ETHICON ENDO-SURGERYOPTICAL DILATOREthicon Endo-Surgery, Inc.K090183HERCULES 3 STAGE WIRE GUIDED DILATION BALLOONCook EndoscopyK082995SMART DILATORSafestitch MedicalK061937COOK ENDOSCOPY ESOPHAGEAL DILATION BALLOONCook EndoscopyK061787MAXFORCE TTS SINGLE-USE BALLOON DILATORBoston Scientific Corp

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.

↑