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Data / Medical devices / United States / Med Labs, Inc.

Med Labs, Inc.: FDA-registered device maker in Goleta, CA, United States, 1 510(k) clearance

Med Labs, Inc. is registered with the FDA (registration 2026803) in Goleta, CA, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 6, 1996. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
2026803
Address
7334 Hollister Ave Ste G, Goleta, CA, United States, 93117
Owner or operator
MED LABS, INC. (2026803)
Roles
Manufacturer
First device listed
October 13, 1992
Registered through
2026
Brand names listed
E-Z CALL, EMS-1C and EMS-2C, PA-1 (PORTABLE ALARM FOR E-Z CALL), SCAN COM (VARIOUS MODELS)

Devices it lists

DeviceProduct codeClassRoleSource
Stimulator, Muscle, PoweredIPF2Manufactureraccessdata.fda.gov
System, Communication, Non-PoweredILP1Manufactureraccessdata.fda.gov
System, Communication, PoweredILQ2Manufactureraccessdata.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
September 6, 1996K960457ELECTRONIC MUSCLE STIMULATOR MODEL EMS-1C/EMS-2CIPFSubstantially EquivalentMed Labs, Inc.accessdata.fda.gov

Compare with other makers

Updated September 6, 1996. 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.