Data / Medical devices / United States / Clinicomp Intl., Inc.
Clinicomp Intl., Inc.: FDA-registered device maker in San Diego, CA, United States, 1 510(k) clearance
Clinicomp Intl., Inc. is registered with the FDA (registration 2028916) in San Diego, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 29, 1995. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2028916
- FEI number
- 1000142646
- Address
- 9655 Towne Centre Dr, San Diego, CA, United States, 92121
- Owner or operator
- CLINICOMP INTL., INC. (9007746)
- Roles
- Manufacturer
- First device listed
- March 28, 2008
- Registered through
- 2026
- Brand names listed
- Fetal Monitor Remote Display
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Monitoring, Perinatal | HGM | 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 |
|---|---|---|---|---|---|---|
| March 29, 1995 | K931133 | CLINICAL INFOR SYST(CIS) W/FETAL MONIT REMOTE DISP | HGM | Substantially Equivalent | Clinicomp, Inc. | accessdata.fda.gov |
Compare with other makers
Updated March 29, 1995. 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.