GVS TM, Inc
Covina, CA, US
GVS TM, INC. appears in FDA device records in Covina, CA. FDA records list no 510(k) clearances, 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
No 510(k) clearance records for this company in the ingested FDA data.
No 510(k) clearance records in the ingested FDA data.
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3037389071 | 2013342 | GVS TM, INC. | 1630 W Industrial Park St, Covina, CA 91722 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- KSRContainer, Empty, For Collection & Processing Of Blood & Blood Components
- JODFilter, Blood, Cardiotomy Suction Line, Cardiopulmonary Bypass
- CAKMicrofilter, Blood Transfusion
- ORGPlatelet And Plasma Separator For Bone Graft Handling
- GKTSeparator, Automated, Blood Cell, Diagnostic
- KSBSet, Transfer (Blood/Plasma)
- KSSSupplies, Blood-Bank
- MZCSystem, Detection, Bacterial, For Platelet Transfusion Products
Recall records
| Recall | Product | Reason | Classification | Initiated | Status |
|---|---|---|---|---|---|
| Z-1157-2026 | SQ40S Blood Transfusion Filter | Due to products being released for distribution prior to completion of the required quality control release process the sterility assurance cannot be confirmed. | Class II | Open, Classified |
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain
