NU-THOR THORACOSTOMY KIT— 510(k) K842666

Name: FDA 510(k) clearance K842666
Creator: U.S. Food and Drug Administration
Published: 1984-09-20

Substantially Equivalent

Intl. Medical Devices , Ltd.

FDA 510(k) clearance K842666 for NU-THOR THORACOSTOMY KIT, Substantially Equivalent on 1984-09-20. Applicant: Intl. Medical Devices , Ltd.. Device class: 1.

Clearance details

Applicant: Intl. Medical Devices , Ltd.
Product code: Code KGZ
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1984-07-10
Decision date: 1984-09-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Monroeville, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KGZ

view all

K022306 — AART SILICONE TUBING2002-10-10
K974295 — BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBING1998-02-10
K973183 — WOUND DRAINAGE HOLDER1998-01-23
K955433 — DURALASTIC SILICONE TUBING1996-01-26
K942315 — NAVARRE PERCUTANEOUS ACCESS SET1994-07-08

More clearances from Intl. Medical Devices , Ltd.

view all

K913540 — PEDIA-THOR THORACOSTOMY KIT1992-04-09
K913541 — NEO-THOR THORACOSTOMY KIT1992-04-09
K913539 — THORACIC CATHTER STYLET1992-01-21
K913542 — THORACIC CATHETER WITH GUIDE1992-01-21
K913543 — THORACIC CATHETER STYLET1991-10-04

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