Pacific Consolidated Industries LLC
Riverside, CA, US
PACIFIC CONSOLIDATED INDUSTRIES, LLC appears in FDA device records in Riverside, CA. FDA records list 6 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show one recall for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 6 510(k) clearances for Pacific Consolidated Industries LLC between 1990 and 2011. The busiest year on record is 1990, with 1. The most recent is 2011, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1990 | 1 |
| 1991 | 1 |
| 2002 | 1 |
| 2004 | 1 |
| 2007 | 1 |
| 2011 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K100957 | DEPLOYABLE OXYGEN CONCENTRATION SYSTEM (DOCS), MODEL 66, DEPLOYABLE OXYGEN CEONCENTRATION | CAW | Substantially Equivalent | |
| K061414 | EXPEDITIONARY DELPLOYABLE OXYGEN CONCENTRATION SYSTEM (EDOCS), MODELS 120B AND 30;MOBILE OXYGEN STORAGE TANK (MOST), MOD | CAW | Substantially Equivalent | |
| K040738 | MOBILE OXYGEN STORAGE TANK (MOST) | CAW | Substantially Equivalent | |
| K020330 | DEPLOYABLE OXYGEN CONCENTRATION SYSTEM (DOCS) | CAW | Substantially Equivalent | |
| K904639 | GENOX MODEL CT-1 | CAW | Substantially Equivalent | |
| K904002 | GENOX MODEL CT-1 OXYGEN/NITROGEN GENER-DISTR SYST | CAW | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 2032532 | 3002768081 | PACIFIC CONSOLIDATED INDUSTRIES, LLC | 12201 MAGNOLIA AVE, Riverside, CA 92503 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
| Recall | Product | Reason | Classification | Initiated | Status |
|---|---|---|---|---|---|
| Z-2201-2008 | Pacific Consolidated Industries Mobile Oxygen Storage Tank, MOST 20-2B, Part Number: 793080-002 | The 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. | Terminated |
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain