LIQUET MEDICAL INC.

FDA Device Registration & Listing · Glen Allen, VA, US · Registration 3038791046

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3038791046
FEI Number
3038791046
Entity Name
LIQUET MEDICAL INC.
City/State/Country
Glen Allen, VA, US
Establishment Address
5619 Country Hills Ln, Glen Allen, VA 23059, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Liquet Medical Inc. (Owner Number: 10093653)
Owner / Operator Contact Address
5619 Country Hills Ln, Glen Allen, VA 23059, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K241851
PMA Number
N/A

All Registered Proprietary Names

Versus Catheter VS110-8B

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DQO Catheter, Intravascular, Diagnostic Cardiovascular Class 2 870.1200 2025-06-17
KRA Catheter, Continuous Flush Cardiovascular Class 2 870.1210 2025-06-17
DYG Catheter, Flow Directed Cardiovascular Class 2 870.1240 2025-06-17
QEY Mechanical Thrombolysis Catheter Cardiovascular Class 2 870.5150 2025-06-17

Official Correspondent

John Schindler

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Liquet Medical Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K151126 Colibri Technologies, Inc. Foresight Intracardiac Echocardiography (ICE) System 2015-12-18
K931629 Carapace, Inc. CARAPACE ANGIOGRAPHY TRAYS 1993-12-06
K823758 Access Devices, Inc. CENTRAL VEIN CATHERIZATION KIT 1983-02-23
K192019 ABBOTT MEDICAL Dragonfly OpStar™ Imaging Catheter, AptiVue™ Software version E.5.1 2019-11-08
K230411 ABBOTT MEDICAL Dragonfly OpStar™ Imaging Catheter 2023-04-14

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3038791046. Last updated year: 2026. Please use registration number 3038791046 when referencing this establishment in official correspondence.
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