SENORAD MULTI-LUMEN BALLOON SOURCE APPLICATOR FOR BRANCHYTHERAPY— 510(k) K071229

Name: FDA 510(k) clearance K071229
Creator: U.S. Food and Drug Administration
Published: 2007-05-18

Unknown

Senorx, Inc.

FDA 510(k) clearance K071229 for SENORAD MULTI-LUMEN BALLOON SOURCE APPLICATOR FOR BRANCHYTHERAPY, Unknown on 2007-05-18. 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: 2007-05-03
Decision date: 2007-05-18
Decision: Unknown
Clearance type: Traditional
Location: Aliso Viejo, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JAQ

view all

K262383 — LumenCare Azure2026-07-24
K252717 — MAASTRO Rectal Applicator Set2026-05-20
K251037 — Rectal Applicator2025-12-19
K252884 — Guided Aarhus Applicator Set2025-11-19
K250299 — CT/ MR Tandem and Ovoid Set2025-05-09

More clearances from Senorx, Inc.

view all

K233220 — EnCor EnspireBreast Biopsy System (E4115, E4230) +4 more2023-10-27
K210654 — EnCor Breast Biopsy Probe with Rinse Tube2021-03-31
K161805 — EnCor MRI Introducer Set, EnCor Probe Introducer2016-07-19
K131654 — STARCHMARK BREAST TISSUE MARKER; STARCHMARK ULTRACOR BREAST TISSUE MARKER2013-06-27
K093512 — ENCOR BREAST BIOPSY SYSTEM2009-11-20

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