510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K931005Substantially Equivalent

Dukal Skin Closure Strip

Dukal Corp., Clinton NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K931005 is the FDA 510(k) clearance record for DUKAL SKIN CLOSURE STRIP, a class I device, cleared for Dukal Corp. on under FDA product code FPX (Strip, Adhesive, Closure, Skin). FDA records list one 510(k) clearance for Dukal Corp. As of , FDA records show no recalls naming K931005.

Clearance record

Decision date
Received
(138 days to decision)
Product code
FPX Strip, Adhesive, Closure, Skin
Regulation
21 CFR 880.5240
Device class
Class I
Review panel
General Hospital
Applicant
Dukal Corp. 17 Crossway, Clinton NJ
510(k) summary
Statement
Third party review
No

Clearances, product code FPX

Trailing 12 months

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

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