Data / Medical devices / United States / Interrad Medical Inc
Interrad Medical Inc: FDA-registered device maker in Minneapolis, MN, United States, 4 510(k) clearances
Interrad Medical Inc is registered with the FDA (registration 3007795799) in Minneapolis, MN, United States. It lists 2 device types. The FDA files 4 510(k) clearances under its listings, the newest dated April 12, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007795799
- Address
- 181 Cheshire Ln N Ste 100, Minneapolis, MN, United States, 55441
- Owner or operator
- Interrad Medical Inc (10027579)
- Roles
- Manufacturer
- First device listed
- October 9, 2012
- Registered through
- 2026
- Brand names listed
- SecurAcath
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Intravascular Catheter Securement | KMK | 1 | Manufacturer | accessdata.fda.gov |
| Implanted Subcutaneous Securement Catheter | OKC | 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 |
|---|---|---|---|---|---|---|
| April 12, 2021 | K210629 | SecurAcath | OKC | Substantially Equivalent | Interrad Medical, Inc. | accessdata.fda.gov |
| July 9, 2019 | K180994 | SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8F | KMK | Substantially Equivalent | Interrad Medical, Inc. | accessdata.fda.gov |
| June 26, 2018 | K180769 | SecurAcath | OKC | Substantially Equivalent | Interrad Medical, Inc. | accessdata.fda.gov |
| April 27, 2012 | K120935 | SECURACATH | OKC | Substantially Equivalent | Interrad Medical, Inc. | accessdata.fda.gov |
Compare with other makers
Updated April 12, 2021. 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.