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FDA 510(k)

MOLLRING CUTTER

K-Number: K950813 · 1995-07-25

ApplicantCardio Vascular Concepts, Inc.
Decision Date1995-07-25
Product CodeDWX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MOLLRING CUTTER is the device name listed in this FDA 510(k) record. The listed applicant is Cardio Vascular Concepts, Inc.. It received FDA 510(k) clearance on 1995-07-25 under 510(k) number K950813. The device is classified under product code DWX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOLLRING CUTTER?

MOLLRING CUTTER is a medical device that received FDA 510(k) clearance on 1995-07-25. The listed applicant is Cardio Vascular Concepts, Inc.. The 510(k) number is K950813.

When did MOLLRING CUTTER receive FDA 510(k) clearance?

MOLLRING CUTTER received FDA 510(k) clearance on 1995-07-25, under 510(k) number K950813.

Who is the listed applicant for MOLLRING CUTTER?

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

What is the FDA product code for MOLLRING CUTTER?

The FDA product code for MOLLRING CUTTER is DWX.

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 Cardio Vascular Concepts, 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.

K950155RAPID-TRAK(TM) INTRODUCER SHEATH

Related Devices (Code: DWX)

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.

K121415MOLLRING MULTITASCLeMaitre Vascular, Inc.K032105ENDOHELIX ENDARTERECTOMY DEVICEEndarx, Inc.K020925CARBODISSECTING ENDOSCOPEEndo Surgical Devices, Inc.K003719VASCULAR ARCHITECTS PERISCOPE DEVICEVascular Architects, Inc.K933498EXTERNAL VEIN STRIPPERApplied Medical ResourcesK913803INTRALUMINAL ARTERY STRIPPEROmni-Tract Surgical, Div. Minn. Scientific, Inc.

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.

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