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Data / Medical devices / United States / Myriad Medical LLC

Myriad Medical LLC: FDA-registered device maker in Tampa, FL, United States, 1 510(k) clearance

Myriad Medical LLC is registered with the FDA (registration 3008513105) in Tampa, FL, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 31, 2015. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3008513105
Address
2202 N West Shore Blvd Ste 200, Tampa, FL, United States, 33607
Owner or operator
Myriad Medical LLC (10032889)
Roles
Specification developer
First device listed
June 22, 2010
Registered through
2026
Brand names listed
ProCradle, Prostate Caddy

Devices it lists

DeviceProduct codeClassRoleSource
Probe, Rectal, Non-PoweredEXX1Specification developeraccessdata.fda.gov
Prostate Immobilizer Rectal BalloonPCT2Specification developeraccessdata.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
March 31, 2015K150234Myriad Prostate Caddy¿ Immobilization Rectal Balloon Item #9901,3301PCTSubstantially EquivalentMyriad Medical, LLCaccessdata.fda.gov

Compare with other makers

Updated March 31, 2015. 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.