510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K842666Substantially Equivalent

Nu-Thor Thoracostomy Kit

Intl. Medical Devices, Ltd., Monroeville PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K842666 is the FDA 510(k) clearance record for NU-THOR THORACOSTOMY KIT, a class I device, cleared for Intl. Medical Devices , Ltd. on under FDA product code KGZ (Accessories, Catheter). FDA records list 12 510(k) clearances for Intl. Medical Devices , Ltd., from to . As of , FDA records show no recalls naming K842666.

Clearance record

Decision date
Received
(72 days to decision)
Product code
KGZ Accessories, Catheter
Regulation
21 CFR 878.4200
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Intl. Medical Devices , Ltd. 530 Seco Rd., Monroeville PA
Third party review
No

Clearances, product code KGZ

Trailing 12 months

FDA records hold no clearances under product code KGZ in the trailing twelve months.

FDA records show no clearances under product code KGZ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KGZ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260