Data / Medical devices / Mexico / GVS Filter Technology De Mexico
GVS Filter Technology De Mexico: FDA-registered device maker in Apodaca N.L Nuevo Leon, Mexico, 3 510(k) clearances
GVS Filter Technology De Mexico is registered with the FDA (registration 3017174574) in Apodaca N.L Nuevo Leon, Mexico. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated May 13, 2004. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017174574
- Address
- Universal #550, Vynmsa airport industrial park, Apodaca N.L Nuevo Leon, Mexico, 66626
- Owner or operator
- GVS Filter Technology de Mexico (10075266)
- Roles
- Manufacturer
- First device listed
- June 10, 2020
- Registered through
- 2026
- Brand names listed
- 100-0016, 100-0024, 100-0034, 100-0040, 100-0121, 100-0139, 100-0147, 100-0167 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Filter, Bacterial, Breathing-Circuit | CAH | 2 | Manufacturer | accessdata.fda.gov |
| Microfilter, Blood Transfusion | CAK | 2 | Manufacturer | accessdata.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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 13, 2004 | K033008 | AIR SAFETY HEPA AND NON-HEPA FILTERS | CAH | Substantially Equivalent | Air Safety, Ltd. | accessdata.fda.gov |
| April 22, 1996 | K960993 | PALL SQ40S BLOOD FILTER (SQ40S/SQ40ST) | CAK | Substantially Equivalent | Pall Biomedical Products Co. | accessdata.fda.gov |
| January 6, 1988 | K873666 | PALL LEUKOCYTE REMOVAL FILTER, BLOOD | CAK | Substantially Equivalent | Pall Biomedical Products Co. | accessdata.fda.gov |
Compare with other makers
Updated May 13, 2004. 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.