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FDA 510(k)

VF LIQUIGEL

K-Number: K083783 · 2009-09-11

ApplicantCoapt Systems, Inc.
Decision Date2009-09-11
Product CodeMIX
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

VF LIQUIGEL is the device name listed in this FDA 510(k) record. The listed applicant is Coapt Systems, Inc.. It received FDA 510(k) clearance on 2009-09-11 under 510(k) number K083783. The device is classified under product code MIX. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VF LIQUIGEL?

VF LIQUIGEL is a medical device that received FDA 510(k) clearance on 2009-09-11. The listed applicant is Coapt Systems, Inc.. The 510(k) number is K083783.

When did VF LIQUIGEL receive FDA 510(k) clearance?

VF LIQUIGEL received FDA 510(k) clearance on 2009-09-11, under 510(k) number K083783.

Who is the listed applicant for VF LIQUIGEL?

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

What is the FDA product code for VF LIQUIGEL?

The FDA product code for VF LIQUIGEL is MIX.

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 Coapt Systems, 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.

K080956MODIFICATION TO VF GEL PLUSK071663VF GEL PLUSK060248ULTRATINE TRANSBLEPHK060249ULTRATINE FOREHEADK060828MODIFICATION TO ENDOTINE RIBBONK051415ENDOTINE RIBBON

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Related Devices (Code: MIX)

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.

K240919Silk Voice (SMI-04)Sofregen MedicalK180631Silk VoiceSofregen Medical, Inc.K121795CALCIUM HYDROXYLAPATITE VOCAL FOLD IMPLANTCytophil, Inc.K081816VOCALIS AND VOCALIS SMCytophil, Inc.K081815VOCALIS GELCytophil, Inc.K080956MODIFICATION TO VF GEL PLUSCoapt Systems, 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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