HIGH DOSE RATE REMOTE AFTERLOADING CATHETER— 510(k) K923738

Name: FDA 510(k) clearance K923738
Creator: U.S. Food and Drug Administration
Published: 1993-04-13

Substantially Equivalent

Cook, Inc.

FDA 510(k) clearance K923738 for HIGH DOSE RATE REMOTE AFTERLOADING CATHETER, Substantially Equivalent on 1993-04-13. Applicant: Cook, Inc.. Device class: 2.

Clearance details

Applicant: Cook, Inc.
Product code: Code JAQ
Device class: Class 2
Regulation: 21 CFR 892.5700
Advisory panel: Radiology
Date received: 1992-07-27
Decision date: 1993-04-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bloomington, IN, 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 Cook, Inc.

view all

K133130 — BEACON TIP TORCON NB ADVANTAGE CATHETER, TORCON NB ADVANTAGE CATHETER2015-01-09
K140593 — ADVANCE SALIVARY BALLOON CATHETER WITH WIRE GUIDE2014-12-15
K132592 — FLEXOR RADIAL HYDROPHILIC INTRODUCER ACCESS SET2014-10-09
K133597 — CIAGLIA PERCUTANEOUS TRACHEOSTOMY INTRODUCER SET/TRAY, CIAGLIA BLUE RHINO PERCUTANEOUS TRACHEOSTOMY INTRODUCER SET/TRAY2014-04-18
K131772 — CANTATA(R) 2.9 MICROCATHETER2014-02-20

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