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FDA 510(k)

NICOLET VASOGUARD

K-Number: K002766 · 2000-11-30

ApplicantNicolet Biomedical
Decision Date2000-11-30
Product CodeJOP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NICOLET VASOGUARD is the device name listed in this FDA 510(k) record. The listed applicant is Nicolet Biomedical. It received FDA 510(k) clearance on 2000-11-30 under 510(k) number K002766. The device is classified under product code JOP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NICOLET VASOGUARD?

NICOLET VASOGUARD is a medical device that received FDA 510(k) clearance on 2000-11-30. The listed applicant is Nicolet Biomedical. The 510(k) number is K002766.

When did NICOLET VASOGUARD receive FDA 510(k) clearance?

NICOLET VASOGUARD received FDA 510(k) clearance on 2000-11-30, under 510(k) number K002766.

Who is the listed applicant for NICOLET VASOGUARD?

The FDA 510(k) record lists Nicolet Biomedical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NICOLET VASOGUARD?

The FDA product code for NICOLET VASOGUARD is JOP.

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 Nicolet Biomedical 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.

K020754NICOLET PIONEER TC8080K013281VERSALAB APMK013419NICOLET ELECTROMAGNETIC NAVIGATION SYSTEMK011135GSI AUDERAK010521NICOLET VERSALABK993939NICOLET EME LEGEND TC22

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Related Devices (Code: JOP)

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.

K242662Falcon/Xpress (Falcon/Xpress)Viasonix , Ltd.K233976VasoGuard (V10, V8, V6, V4, V2)Corvascular Diagnostics, LLCK153762Smartdop XT6Koven Technology, Inc.K131860VASCULAB VL4000 PHOTOPLETHYSMOGRAPH WITH PULSE VOLUME RECORDINGUs Vascular, LLCK111416FALCONViasonix , Ltd.K071730STUDIODOP VICORDERSkidmore Medical, Limited

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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