510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K874645Substantially Equivalent

Closed Wound Drainage Systems

Hall Laboratories, Inc., Merriam KS / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K874645 is the FDA 510(k) clearance record for CLOSED WOUND DRAINAGE SYSTEMS, a class I device, cleared for Hall Laboratories, Inc. on under FDA product code GCY (Apparatus, Suction, Single Patient Use, Portable, Nonpowered). FDA records list 2 510(k) clearances for Hall Laboratories, Inc., from to . As of , FDA records show no recalls naming K874645.

Clearance record

Decision date
Received
(19 days to decision)
Product code
GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered
Regulation
21 CFR 878.4680
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Hall Laboratories, Inc. 9900 Camino Royal #91, Merriam KS
Third party review
No

Clearances, product code GCY

Trailing 12 months

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

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