Interrad Medical Inc
Minneapolis, MN, US
Interrad Medical Inc appears in FDA device records in Minneapolis, MN. FDA records list 7 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 7 510(k) clearances for Interrad Medical Inc between 2008 and 2021. The busiest year on record is 2008, with 1. The most recent is 2021, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2008 | 1 |
| 2009 | 1 |
| 2010 | 1 |
| 2012 | 1 |
| 2018 | 1 |
| 2019 | 1 |
| 2021 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K210629 | SecurAcath | OKC | Substantially Equivalent | |
| K180994 | SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8F | KMK | Substantially Equivalent | |
| K180769 | SecurAcath | OKC | Substantially Equivalent | |
| K120935 | SECURACATH | OKC | Substantially Equivalent | |
| K092306 | SECURACATH UNIVERSAL | LJS | Substantially Equivalent | |
| K083081 | MODIFICATION TO SECURACATH, MODEL: SPK01 | OKC | Substantially Equivalent | |
| K082047 | SECURACATH CATHETER, MODEL SPK01 | OKC | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3007795799 | 3007795799 | Interrad Medical Inc | 181 Cheshire Ln N Ste 100, Minneapolis, MN 55441 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain