Data / Medical devices / Panama / Outsourcing Farm La, Corp
Outsourcing Farm La, Corp: FDA-registered device maker in Panama, Panama, 1 510(k) clearance
Outsourcing Farm La, Corp is registered with the FDA (registration 3017088037) in Panama, Panama. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 7, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017088037
- Address
- Calle 8va. Galera Corregimiento Rio Abajo 22, Panama, Panama, Panama, Panama, Panama, 0801-01201
- Owner or operator
- Outsourcing Farm LA, Corp (10095149)
- Roles
- Specification developer
- First device listed
- January 28, 2026
- Registered through
- 2026
- Brand names listed
- JR-009-AU 60 PSI Needleless Neutral Valve, JR-009-HU 300 PSI High-Pressure Needleless Neutral Valve, JR-009-TU 60 PSI Transparent Needleless Neutral Valve, JR-009M Equipo de Infusion con Valvula Libre de Aguja - Valvula Neutra Libre de Aguga 60 psi, JR-010-AU Biosite Surgical Set, JR-010-BU Biosite Surgical Set, JR-010-RU Biosite Surgical Set, JR-010M Equipo de Infusion con Valvula Libre de Aguja - Biosite Macro Quirurgico and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Set, Administration, Intravascular | FPA | 2 | Specification developer | 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 7, 2013 | K121511 | MACLIN POWER INTRAVASCULAR ADMINISTRATION SET | FPA | Substantially Equivalent | Maclin Power, Inc. | accessdata.fda.gov |
Compare with other makers
Updated March 7, 2013. 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.