Data / Medical devices / United States / Diagnostic Consulting Network, LLC.
Diagnostic Consulting Network, LLC.: FDA-registered device maker in Carlsbad, CA, United States, 2 510(k) clearances
Diagnostic Consulting Network, LLC. is registered with the FDA (registration 2951280) in Carlsbad, CA, United States. It lists 5 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 16, 1999. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2951280
- FEI number
- 1000221318
- Address
- 3193 Lionshead Ave. Suite 200, Carlsbad, CA, United States, 92010
- Owner or operator
- Diagnostic Consulting Network, LLC. (10087060)
- Roles
- Manufacturer
- First device listed
- January 6, 2023
- Registered through
- 2026
- Brand names listed
- JSG, JSI, JSJ, JSN, JTY
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Culture Media, For Isolation Of Pathogenic Neisseria | JTY | 2 | Manufacturer | accessdata.fda.gov |
| Culture Media, Non-Selective And Non-Differential | JSG | 1 | Manufacturer | accessdata.fda.gov |
| Culture Media, Propagating Transport | JSN | 1 | Manufacturer | accessdata.fda.gov |
| Culture Media, Selective And Differential | JSI | 1 | Manufacturer | accessdata.fda.gov |
| Culture Media, Selective And Non-Differential | JSJ | 1 | 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 |
|---|---|---|---|---|---|---|
| December 16, 1999 | K993033 | INTRAY GC | JTY | Substantially Equivalent | Biomed Diagnostics, Inc. | accessdata.fda.gov |
| January 29, 1990 | K896296 | INPOUCH-TV POUCH | JSN | Substantially Equivalent | Biomed Diagnostics, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Culture Media, Selective And Non-Differential
- All makers of Culture Media, For Isolation Of Pathogenic Neisseria
- All makers of Culture Media, Propagating Transport
- All makers of Culture Media, Non-Selective And Non-Differential
- All makers of Culture Media, Selective And Differential
Updated December 16, 1999. 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.