CONTURA CAVITY MAINTENANCE CATHETER— 510(k) K092323

Name: FDA 510(k) clearance K092323
Creator: U.S. Food and Drug Administration
Published: 2009-08-19

Substantially Equivalent

Senorx, Inc.

FDA 510(k) clearance K092323 for CONTURA CAVITY MAINTENANCE CATHETER, Substantially Equivalent on 2009-08-19. Applicant: Senorx, Inc.. Device class: 2.

Clearance details

Applicant: Senorx, Inc.
Product code: Code JAQ
Device class: Class 2
Regulation: 21 CFR 892.5700
Advisory panel: Radiology
Date received: 2009-08-04
Decision date: 2009-08-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.