Amico Patient Care Corporation

FDA Device Registration & Listing · Richmond Hill Ontario, CA · Registration 3009162879

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
3009162879
FEI Number
3012398026
Entity Name
Amico Patient Care Corporation
City/State/Country
Richmond Hill Ontario, CA
Establishment Address
122A East Beaver Creek Rd, Richmond Hill Ontario L4B 1G6, CA
Establishment Type(s)
Manufacture Medical Device,Repack or Relabel Medical Device
Owner / Operator
Amico Patient Care Corporation (Owner Number: 10040486)
Owner / Operator Contact Address
122A East Beaver Creek Rd, Richmond Hill, CA-ON L4B 1G6, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

APC Oxygen Humidifier Bottle, Collection Bottle & Vacuum Trap pediatric hospital bed Vacuum Regulator Dial Flowmeter Flowmeter Bassinet hospital

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CBC Bottle, Collection And Trap, Breathing System (Uncalibrated) General Hospital Class 2 880.6740 2019-07-24
FMS Bed, Pediatric Open Hospital General Hospital Class 2 880.5140 2012-04-19
KDP Regulator, Vacuum General Hospital Class 2 880.6740 2013-02-07
CCN Flowmeter, Nonback-Pressure Compensated, Bourdon Gauge Anesthesiology Class 1 868.2300 2017-03-30
CAX Flowmeter, Tube, Thorpe, Back-Pressure Compensated Anesthesiology Class 1 868.2340 2013-02-07
NZG Bassinet, Hospital General Hospital Class 2 880.5145 2015-07-09

Official Correspondent

Eric Charron

US Agent Details

Jon Ward Business: AJW Technology Consultants, Inc. Email: usagent@ajwtech.com Phone: (813) 6452855

Related Public Records

Same Entity

Amico Patient Care Corporation
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009162879. Last updated year: 2026. Please use registration number 3009162879 when referencing this establishment in official correspondence.
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