Data / Medical devices / United States / Cedars Sinai Medical Center
Cedars Sinai Medical Center: FDA-registered device maker in Los Angeles, CA, United States, 1 510(k) clearance
Cedars Sinai Medical Center is registered with the FDA (registration 3009136051) in Los Angeles, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 3, 2017. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3009136051
- Address
- 6500 Wilshire Blvd, 5th floor, Los Angeles, CA, United States, 90048
- Owner or operator
- Cedars-Sinai Medical Center (10037809)
- Roles
- Manufacturer
- First device listed
- August 6, 2018
- Registered through
- 2027
- Brand names listed
- Cedars-Sinai Cardiac Suite
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Tomography, Computed, Emission | KPS | 2 | Manufacturer | accessdata.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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 3, 2017 | K172609 | CSMC Cardiac Suite | KPS | Substantially Equivalent | Cedars-Sinai Medical Center | accessdata.fda.gov |
Compare with other makers
Updated November 3, 2017. 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.