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
K924337Substantially Equivalent

Pleur-Evac(r) Adult/pedi Dual Coll Chest Drain Sys

Deknatel, Inc., San Jose-Heredia, CR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K924337 is the FDA 510(k) clearance record for PLEUR-EVAC(R) ADULT/PEDI DUAL COLL CHEST DRAIN SYS, a class II device, cleared for Deknatel, Inc. on under FDA product code GCX (Apparatus, Suction, Operating-Room, Wall Vacuum Powered). FDA records list 37 510(k) clearances for Deknatel, Inc., from to . As of , FDA records show no recalls naming K924337.

Clearance record

Decision date
Received
(335 days to decision)
Product code
GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered
Regulation
21 CFR 880.6740
Device class
Class II
Review panel
General Hospital
Applicant
Deknatel, Inc. Kilometer 9 Carretera, San Jose-Heredia, CR
510(k) summary
Summary
Third party review
No

Clearances, product code GCX

Trailing 12 months

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

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