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 STRICTURE MEASURING CATHETER

K-Number: K973205 · 1997-11-24

ApplicantWilson-Cook Medical, Inc.
Decision Date1997-11-24
Product CodeODD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WILSON-COOK STRICTURE MEASURING CATHETER 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 1997-11-24 under 510(k) number K973205. The device is classified under product code ODD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILSON-COOK STRICTURE MEASURING CATHETER?

WILSON-COOK STRICTURE MEASURING CATHETER is a medical device that received FDA 510(k) clearance on 1997-11-24. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K973205.

When did WILSON-COOK STRICTURE MEASURING CATHETER receive FDA 510(k) clearance?

WILSON-COOK STRICTURE MEASURING CATHETER received FDA 510(k) clearance on 1997-11-24, under 510(k) number K973205.

Who is the listed applicant for WILSON-COOK STRICTURE MEASURING CATHETER?

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 STRICTURE MEASURING CATHETER?

The FDA product code for WILSON-COOK STRICTURE MEASURING CATHETER is ODD.

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: ODD)

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.

K250573Single Use Cannula V PR-V223Q/V414Q/V416Q/V418Q/V420Q/V427Q/V434Q/V435Q; Single Use 2-Lumen Cannula V PR-V614MOlympus Medical Systems Corp.K202583BioShield biopsy valve EUS - LinearSTERIS CorporationK171989Classic ERCP Catheter and Huibregtse-Katon ERCP Catheter and Huibregtse-Katon Angled, Glo-Tip ERCP Catheter, Glo-Tip II Double Lumen ERCP Catheter & w/ Radiopaque Bands, Fusion ERCP Catheter with DomeTip and Fusion OMNI ERCP Catheter with DomeTip, Haber RAMP Catheter, Soehendra Universal CatheterWilson-Cook Medical, Inc.K070420BIOSHIELD-ERCP BIOPSY VALVE, MODEL 00711138United States Endoscopy Group, Inc.K011149DISPOSABLE BENDING CANNULA PR-233QThe Olympus Optical Co.K010993ALIEN RX MICRO CANNULA, MODEL 4530Boston 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.

↑