Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K914174Unknown

Sterile Disposable Wet Skin Scrub Tray

Medical Device Inspection Company, Great Neck NY / Traditional, Unknown

K914174 is the FDA 510(k) clearance record for STERILE DISPOSABLE WET SKIN SCRUB TRAY, a class II device, cleared for Medical Device Inspection Co., Inc. on under FDA product code LRO (General Surgery Tray). FDA's definition for product code LRO reads: "This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the...". FDA records list 30 510(k) clearances for Medical Device Inspection Co., Inc., from to . As of , FDA records show one recall naming K914174.

Clearance record

Decision date
Received
(159 days to decision)
Product code
LRO General Surgery Tray
Regulation
21 CFR 878.4370
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Medical Device Inspection Co., Inc. 55 Northern Blvd., Suite 301, Great Neck NY
510(k) summary
Statement
Third party review
No

Clearances, product code LRO

Trailing 12 months

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

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