SecurAcath— 510(k) K210629

Substantially Equivalent

Interrad Medical, Inc.

FDA 510(k) clearance K210629 for SecurAcath, Substantially Equivalent on 2021-04-12. Applicant: Interrad Medical, Inc.. Device class: 2.

Clearance details

Applicant: Interrad Medical, Inc.
Product code: Code OKC
Device class: Class 2
Regulation: 21 CFR 880.5970
Advisory panel: General Hospital
Date received: 2021-03-02
Decision date: 2021-04-12
Decision: Substantially Equivalent
Clearance type: Special
Location: Plymouth, MN, US

Download summary PDF View on FDA.gov ↗

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