510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K903073Substantially Equivalent

Latex Finger Cots

Dongkuk Trading Co., Ltd., Seoul, Korea, KR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K903073 is the FDA 510(k) clearance record for LATEX FINGER COTS, a class I device, cleared for Dongkuk Trading Co., Ltd. on under FDA product code LZB (Finger Cot). FDA records list one 510(k) clearance for Dongkuk Trading Co., Ltd. As of , FDA records show no recalls naming K903073.

Clearance record

Decision date
Received
(62 days to decision)
Product code
LZB Finger Cot
Regulation
21 CFR 880.6250
Device class
Class I
Review panel
General Hospital
Applicant
Dongkuk Trading Co., Ltd. K.P.O Box 150, Seoul, Korea, KR
Third party review
No

Clearances, product code LZB

Trailing 12 months

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

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