Millar LLC.

FDA Device Registration & Listing · Houston, TX, US · Registration 3027605168

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
3027605168
FEI Number
1625382
Entity Name
Millar LLC.
City/State/Country
Houston, TX, US
Establishment Address
11950 N. Spectrum, --, Houston, TX 77047, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Millar LLC (Owner Number: 1625382)
Owner / Operator Contact Address
11950 N. Spectrum, --, Houston, TX 77047, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K842150
PMA Number
N/A

All Registered Proprietary Names

Transduce Signal Amplifier PCU-2000 Mikro-Cath Pressure Catheter Micro-Tip Catheter Pulse Transducer Transducer Monitor Interface-TC-510

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GWM Device, Monitoring, Intracranial Pressure Neurology Class 2 882.1620 2024-08-29
DRQ Amplifier And Signal Conditioner, Transducer Signal Cardiovascular Class 2 870.2060 2008-07-22
DXO Transducer, Pressure, Catheter Tip Cardiovascular Class 2 870.2870 2010-05-12
DXO Transducer, Pressure, Catheter Tip Cardiovascular Class 2 870.2870 2008-07-22
DXO Transducer, Pressure, Catheter Tip Cardiovascular Class 2 870.2870 2008-07-22

Official Correspondent

Jacqueline Jean-Baptiste

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Millar LLC
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
K020558 Integra Neurosciences LICOX CC1.G2 BRAIN OXYGEN CATHETER-MICROPROBE 2002-03-21

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027605168. Last updated year: 2026. Please use registration number 3027605168 when referencing this establishment in official correspondence.
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