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)

S/2(TM) STOPCOCK

K-Number: K926423 · 1993-03-23

ApplicantPsi Medical Products, Inc.
Decision Date1993-03-23
Product CodeFGB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

S/2(TM) STOPCOCK is the device name listed in this FDA 510(k) record. The listed applicant is Psi Medical Products, Inc.. It received FDA 510(k) clearance on 1993-03-23 under 510(k) number K926423. The device is classified under product code FGB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the S/2(TM) STOPCOCK?

S/2(TM) STOPCOCK is a medical device that received FDA 510(k) clearance on 1993-03-23. The listed applicant is Psi Medical Products, Inc.. The 510(k) number is K926423.

When did S/2(TM) STOPCOCK receive FDA 510(k) clearance?

S/2(TM) STOPCOCK received FDA 510(k) clearance on 1993-03-23, under 510(k) number K926423.

Who is the listed applicant for S/2(TM) STOPCOCK?

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

What is the FDA product code for S/2(TM) STOPCOCK?

The FDA product code for S/2(TM) STOPCOCK is FGB.

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 Psi Medical Products, 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.

K931779EHL PULSE GENERATORK915459FLOWMATE HAND PUMPK920410EMILITH ELECTROMECHANICALIMPACTOR LITHOTRIPSY PROBK921415IRRIGATION TUBING SETK921253INSTRUMENT IRRIGATION PUMPK915458URETEROSCOPE

View all 7 devices →

Related Devices (Code: FGB)

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.

K261447CVAC® Aspiration SystemCalyxo, Inc.K262488Single-Use Video Flexible Ureterorenoscope (RP-U-C06R9, RP-U-C06R3, RP-U-C06S9, RP-U-C06S3)Guangzhou Red Pine Medical Instrument Co., Ltd.K261153LithoVue Elite Digital Flexible Ureteroscope SystemBoston Scientific CorporationK262552Single-use Flexible Ureteroscope (Single-use Flexible Ureteroscope: SUV-5C-B)Scivita Medical Technology Co., Ltd.K253505Zamenix™ PRoen Surgical, Inc.K260516BubbleView Single-Use Digital Flexible Cystoscope (C38-CS, C38-CRS, C50-C, C50-CR, C50-CB, C50-CBR)MacroLux Medical Technology Co., 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.

↑