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Data / Medical devices / United States / Med Systems

Med Systems: FDA-registered device maker in San Diego, CA, United States, 1 510(k) clearance

Med Systems is registered with the FDA (registration 2022691) in San Diego, CA, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 21, 2003. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
2022691
Address
2631 Ariane DR., San Diego, CA, United States, 92117
Owner or operator
MED SYSTEMS (2022691)
Roles
Manufacturer
First device listed
October 20, 1992
Registered through
2026
Brand names listed
ELECTRO FLO PERCUSSOR, FLUID FLOW, MEDS SERIES 2100 MASK

Devices it lists

DeviceProduct codeClassRoleSource
Mask, Gas, AnestheticBSJ1Manufactureraccessdata.fda.gov
PercussorGWZ1Manufactureraccessdata.fda.gov
Percussor, Powered-ElectricBYI2Manufactureraccessdata.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
November 21, 2003K031876ELECTRO FLO PERCUSSOR, MODEL 5000BYISubstantially EquivalentMed Systemsaccessdata.fda.gov

Compare with other makers

Updated November 21, 2003. 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.