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Data / Medical devices / United States / Multi Biosensors, Inc.

Multi Biosensors, Inc.: FDA-registered device maker in El Paso, TX, United States, 2 510(k) clearances

Multi Biosensors, Inc. is registered with the FDA (registration 1640699) in El Paso, TX, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated May 6, 1987. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
1640699
Address
3635 Buckner, El Paso, TX, United States, 79925
Owner or operator
MULTI BIOSENSORS, INC. (1640699)
Roles
Manufacturer
First device listed
March 14, 2008
Registered through
2026
Brand names listed
DISPOSABLE ELECTRODES

Devices it lists

DeviceProduct codeClassRoleSource
Electrode, ElectrocardiographDRX2Manufactureraccessdata.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
May 6, 1987K864690ADDITIONAL USE FOR ECG DISPOSABLE ELECTRODE V-PADDRXSubstantially EquivalentMulti Biosensors, Inc.accessdata.fda.gov
March 1, 1985K842514ELECTROCARDIOGRAM DISPOS. ELECTRODE PADDRXSubstantially EquivalentMulti Biosensors, Inc.accessdata.fda.gov

Compare with other makers

Updated May 6, 1987. 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.