Dukal Corp.
Dukal Corp. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 2009, with 1 FDA device recall on record.
Top product codes for Dukal Corp.
FDA recalls by Dukal Corp.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Dukal Corp.
- K083320 — DUKAL SURGICAL DRAPE; FENESTRATED DUKAL SURGICAL DRAPE
- K070407 — DUKAL SURGICAL FACE MASK TIE, EAR LOOP, WITH SHIELD YELLOW & WHITE; ANTI FOG TIE, LOOP, SHIELD, YELLOW, WHITE, AND BLUE
- K061864 — DUKAL SURGICAL FACE MASK TIE-ON, MODEL 1530; EAR LOOP, MODEL 1540; WITH SHIELD, MODEL 1560
- K020726 — DUKAL DISPOSABLE VAGINAL SPECULUM, SMALL, MEDIUM, AND LARGE
- K984564 — ETHYL CHLORIDE DISPENSER
- K970455 — DUKAL NON ADHERENT DRESSING
- K970457 — DUKAL ABD COMBINE PAD
- K955476 — DUKAL TRANSPARENT WOUND DRESSING
- K940440 — DUKAL NON-WOVEN GAUZE
- K936095 — GAUZE SPONGE
- K931005 — DUKAL SKIN CLOSURE STRIP
Data sourced from openFDA. This site is unofficial and independent of the FDA.