SOURCE PRODUCTION & EQUIPMENT CO, INC., MODEL M-19 IR-192 BRACHYTHERAPY SOURCE— 510(k) K052947

Name: FDA 510(k) clearance K052947
Creator: U.S. Food and Drug Administration
Published: 2006-04-19

Substantially Equivalent

Source Production & Equipment Co., Inc.

FDA 510(k) clearance K052947 for SOURCE PRODUCTION & EQUIPMENT CO, INC., MODEL M-19 IR-192 BRACHYTHERAPY SOURCE, Substantially Equivalent on 2006-04-19. Applicant: Source Production & Equipment Co., Inc.. Device class: 2.

Clearance details

Applicant: Source Production & Equipment Co., Inc.
Product code: Code JAQ
Device class: Class 2
Regulation: 21 CFR 892.5700
Advisory panel: Radiology
Date received: 2005-10-20
Decision date: 2006-04-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Saint Rose, LA, 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 Source Production & Equipment Co., Inc.

view all

K132969 — SPEC MODEL M152014-01-02
K090366 — SPEC MODEL M-312009-04-22

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