McARTHUR MEDICAL SALES, INC.

FDA Device Registration & Listing · ROCKTON, ONTARIO, CA · Registration 9615334

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
9615334
FEI Number
3002705047
Entity Name
McARTHUR MEDICAL SALES, INC.
City/State/Country
ROCKTON, ONTARIO, CA
Establishment Address
1846 5th Concession West, ROCKTON, ONTARIO LOR IX0, CA
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
McARTHUR MEDICAL SALES, INC. (Owner Number: 9021818)
Owner / Operator Contact Address
1846 5th Concession West, Rockton, Ontario, CA-ON LOR IX0, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SPEEDSPLINT Odapt-O2 adapter Flusso By Pass Adapter Flusso By Pass, Flusso TFI Flusso TFI

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NOC Splint, Extremity, Non-Inflatable, External, Non-Sterile General, Plastic Surgery Class 1 878.3910 2008-03-07
BYX Tubing, Pressure And Accessories Anesthesiology Class 1 868.5860 2024-03-14
BZO Set, Tubing And Support, Ventilator (W Harness) Anesthesiology Class 1 868.5975 2020-01-07

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: REGISTRAR CORP Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

McARTHUR MEDICAL SALES, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-2026 Percussionaire Corporation 1
Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF: P5-TEE-20 (pack of 20)/ P5-TEE (individual) with In-Line Valve Sentec Instructions for Use

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9615334. Last updated year: 2026. Please use registration number 9615334 when referencing this establishment in official correspondence.
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