IMPLANT GUIDANCE SYSTEM APPLICATOR SET— 510(k) K020015

Name: FDA 510(k) clearance K020015
Creator: U.S. Food and Drug Administration
Published: 2002-03-13

Substantially Equivalent

Nucletron Corp.

FDA 510(k) clearance K020015 for IMPLANT GUIDANCE SYSTEM APPLICATOR SET, Substantially Equivalent on 2002-03-13. Applicant: Nucletron Corp.. Device class: 2.

Clearance details

Applicant: Nucletron Corp.
Product code: Code JAQ
Device class: Class 2
Regulation: 21 CFR 892.5700
Advisory panel: Radiology
Date received: 2002-01-03
Decision date: 2002-03-13
Decision: Substantially Equivalent
Clearance type: Special
Location: Columbia, MD, 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 Nucletron Corp.

view all

K092804 — MICROSELECTRON HDR V2, MODEL 105.9992009-10-08
K091598 — LUMENCATH APPLICATOR SET, MODELS 189. 795, 189.796, 189.797, 189.798, LUMENCATH CATHETERS2009-06-29
K072445 — INTEGRATED BRACHYTHERAPY UNIT - DIGITAL2007-09-14
K041715 — INTRACAVITARY MOULD APPLICATOR SET, MODEL 189.0012005-03-24
K041933 — MICROSELECTRON PDR2004-08-18

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