Data / Medical devices / Switzerland / pfm medical cpp SA
pfm medical cpp SA: FDA-registered device maker in LA CHAUX-DE-FONDS Neuchatel, Switzerland, 5 510(k) clearances
pfm medical cpp SA is registered with the FDA (registration 9681202) in LA CHAUX-DE-FONDS Neuchatel, Switzerland. It lists 2 device types. The FDA files 5 510(k) clearances under its listings, the newest dated July 16, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9681202
- FEI number
- 3008737795
- Address
- Allee Du Quartz 9, LA CHAUX-DE-FONDS Neuchatel, Switzerland, 2300
- Owner or operator
- PFM Medical (9020573)
- Roles
- Complaint file establishment, Contract manufacturer, Manufacturer
- First device listed
- January 12, 2006
- Registered through
- 2026
- Brand names listed
- JetPort Plus Catheter System, Micro Introducer
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter Introducer Kit | OFC | 2 | Contract manufacturer | accessdata.fda.gov |
| Port & Catheter, Implanted, Subcutaneous, Intravascular | LJT | 2 | Complaint file establishment, 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 |
|---|---|---|---|---|---|---|
| July 16, 2013 | K122402 | LPP (LOW PROFILE PORT) | LJT | Substantially Equivalent | Pfm Medical, Inc. | accessdata.fda.gov |
| March 7, 2008 | K072481 | JET PORT PLUS HP CATHETER SYSTEM | LJT | Substantially Equivalent | Pfm Medical, Inc. | accessdata.fda.gov |
| December 12, 2007 | K073210 | MODIFICATION TO: T-PORT HP INFUSION PORT | LJT | Substantially Equivalent | Pfm Medical, Inc. | accessdata.fda.gov |
| October 17, 2007 | K071993 | T-PORT HP INFUSION PORT | LJT | Substantially Equivalent | Pfm Medical, Inc. | accessdata.fda.gov |
| April 12, 2000 | K000125 | JET PORT PLUS CATHETER SYSTEM | LJT | Substantially Equivalent | Clinical Plastic Products SA | accessdata.fda.gov |
Compare with other makers
- All makers of Port & Catheter, Implanted, Subcutaneous, Intravascular
- All makers of Catheter Introducer Kit
Updated July 16, 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.