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Data / Medical devices / United States / Tulip Medical Products, Inc.

Tulip Medical Products, Inc.: FDA-registered device maker in San Diego, CA, United States, 1 510(k) clearance

Tulip Medical Products, Inc. is registered with the FDA (registration 2030580) in San Diego, CA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 27, 2006. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
2030580
FEI number
1000518699
Address
4360 Morena Blvd, San Diego, CA, United States, 92117
Owner or operator
Tulip Medical Products Inc. (10028110)
Roles
Manufacturer
First device listed
December 30, 2008
Registered through
2027
Brand names listed
Tulip Medical Products

Devices it lists

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
April 27, 2006K060089TULIP DISPOSABLE CANNULASQPBSubstantially EquivalentCell Bio-Systems, Inc.accessdata.fda.gov

Compare with other makers

Updated April 27, 2006. 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.