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Data / Medical devices / United States / Pacific Consolidated Industries, LLC

Pacific Consolidated Industries, LLC: FDA-registered device maker in Riverside, CA, United States, 3 510(k) clearances

Pacific Consolidated Industries, LLC is registered with the FDA (registration 2032532) in Riverside, CA, United States. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated January 21, 2011. 1 recall event names it as the recalling firm. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
2032532
FEI number
3002768081
Address
12201 Magnolia Ave, Riverside, CA, United States, 92503
Owner or operator
PCI GASES (9049531)
Roles
Manufacturer
First device listed
February 5, 2002
Registered through
2027
Brand names listed
Deployable Oxygen Concentration System

Devices it lists

DeviceProduct codeClassRoleSource
Generator, Oxygen, PortableCAW2Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
January 21, 2011K100957DEPLOYABLE OXYGEN CONCENTRATION SYSTEM (DOCS), MODEL 66, DEPLOYABLE OXYGEN CEONCENTRATIONCAWSubstantially EquivalentPacific Consolidated Industries, LLCaccessdata.fda.gov
January 22, 2007K061414EXPEDITIONARY DELPLOYABLE OXYGEN CONCENTRATION SYSTEM (EDOCS), MODELS 120B AND 30;MOBILE OXYGEN STORAGE TANK (MOST), MODCAWSubstantially EquivalentPacific Consolidated Industries, LLCaccessdata.fda.gov
April 30, 2004K040738MOBILE OXYGEN STORAGE TANK (MOST)CAWSubstantially EquivalentPacific Consolidated Industries Llpaccessdata.fda.gov

Recalls

Recall events where this establishment is the recalling firm, matched on its FEI.

InitiatedEventClassStatusProductReasonSource
September 8, 200749030Not yet classifiedTerminatedPacific Consolidated Industries Mobile Oxygen Storage Tank, MOST 20-2B, Part Number: 793080-002The recall was initiated after the firm received two customer complaints of ruptured bourdon tubes that had resulted in bellowed out face gauges. With one unit the operator was able to shut off the oxygen flow, however one rupture resulted in a fire. No injuries were reported.accessdata.fda.gov

Compare with other makers

Updated January 21, 2011. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.