Data / Medical devices / Norway / Memscap AS
Memscap AS: FDA-registered device maker in SKOPPUM Vestfold, Norway, 1 510(k) clearance
Memscap AS is registered with the FDA (registration 8043969) in SKOPPUM Vestfold, Norway. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 7, 1979. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 8043969
- FEI number
- 3004050362
- Address
- Langmyra 11, SKOPPUM Vestfold, Norway, 3185
- Owner or operator
- MEMSCAP AS (9004868)
- Roles
- Manufacturer
- First device listed
- May 3, 2011
- Registered through
- 2026
- Brand names listed
- CPJ84022 Dome sterile; SP840 Physiological pressure transducer / CPJ840J6
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Transducer, Blood-Pressure, Extravascular | DRS | 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 |
|---|---|---|---|---|---|---|
| December 7, 1979 | K792020 | AE 840 PHYSIOLOGICAL PRESSURE TRANSDUCER | DRS | Substantially Equivalent | Life Medical Services, Inc. | accessdata.fda.gov |
Compare with other makers
Updated December 7, 1979. 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.