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)

ROTATING HEMOSTATIC VALVE

K-Number: K883916 · 1988-10-28

ApplicantDevices For Vascular Intervention, Inc.
Decision Date1988-10-28
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ROTATING HEMOSTATIC VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Devices For Vascular Intervention, Inc.. It received FDA 510(k) clearance on 1988-10-28 under 510(k) number K883916. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROTATING HEMOSTATIC VALVE?

ROTATING HEMOSTATIC VALVE is a medical device that received FDA 510(k) clearance on 1988-10-28. The listed applicant is Devices For Vascular Intervention, Inc.. The 510(k) number is K883916.

When did ROTATING HEMOSTATIC VALVE receive FDA 510(k) clearance?

ROTATING HEMOSTATIC VALVE received FDA 510(k) clearance on 1988-10-28, under 510(k) number K883916.

Who is the listed applicant for ROTATING HEMOSTATIC VALVE?

The FDA 510(k) record lists Devices For Vascular Intervention, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ROTATING HEMOSTATIC VALVE?

The FDA product code for ROTATING HEMOSTATIC VALVE is DQY.

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 Devices For Vascular Intervention, 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.

K935929MICROTRACKK920707HOLLOW MOTOR DRIVE UNIT W/ TORQUE CONTROLLERK914422DEVICES FOR VASCU INTERVENT ROTAT HEMOSTAT VALVEK911678ROTATING HEMOSTATIC VALVEK910205LP-60 LOW PRESSURE INFLATION DEVICEK901601HOLLOW MOTOR DRIVE UNIT

View all 14 devices →

Related Devices (Code: DQY)

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.

K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbott

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.

↑