MULTISOURCE MFG. LLC

FDA Device Registration & Listing · Fridley, MN, US · Registration 3011604145

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
3011604145
FEI Number
3011604145
Entity Name
MULTISOURCE MFG. LLC
City/State/Country
Fridley, MN, US
Establishment Address
7500 Commerce Ln., Fridley, MN 55432, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
MULTISOURCE MANUFACTURING LLC (Owner Number: 9055838)
Owner / Operator Contact Address
6690 Sunwood Dr. NW, --, Ramsey, MN 55303, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

DRQ

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DRQ Amplifier And Signal Conditioner, Transducer Signal Cardiovascular Class 2 870.2060 2019-12-13

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MULTISOURCE MANUFACTURING LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Other Registrations for Same Entity

Registration Number Establishment Name Location
3010009632 MULTISOURCE MANUFACTURING LLC Longmont, CO, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011604145. Last updated year: 2026. Please use registration number 3011604145 when referencing this establishment in official correspondence.
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