510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K854293Substantially Equivalent

Medsurg Pott-Cournand Needle

Medsurg Industries, Inc., Herndon VA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K854293 is the FDA 510(k) clearance record for MEDSURG POTT-COURNAND NEEDLE, a class II device, cleared for Medsurg Industries, Inc. on under FDA product code DRC (Trocar). FDA records list 41 510(k) clearances for Medsurg Industries, Inc., from to . As of , FDA records show no recalls naming K854293.

Clearance record

Decision date
Received
(82 days to decision)
Product code
DRC Trocar
Regulation
21 CFR 870.1390
Device class
Class II
Review panel
Cardiovascular
Applicant
Medsurg Industries, Inc. 251 Exchange Pl., Herndon VA
Third party review
No

Clearances, product code DRC

Trailing 12 months

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

FDA records show no clearances under product code DRC in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DRC, 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