Atlas FDA

DUKAL SKIN CLOSURE STRIP

FDA 510(k) clearance K931005 · decided 1993-07-14

Clearance details

K-number
K931005
Device name
DUKAL SKIN CLOSURE STRIP
Applicant
Dukal Corp.
Decision
Substantially Equivalent
Date received
1993-02-26
Decision date
1993-07-14
Days to decision
138 days
Clearance type
Traditional
Product code
FPX
Device class
1
Regulation number
880.5240
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Clinton, NJ, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
K-KLOSURE 2 INCH LENGTH/4 INCH LENGTH/8 INCH LENGTH/12 INCH LENGTH (K970441)Medi-Flex Hospital Products, Inc.1997-05-09
DELPORE SKIN CLOSURE (K952947)Bitco Intl.1995-07-24
DERMA SEAL (K952702)Ttl Medical1995-06-28
BIOSTRIP STERILE WOUND CLOSURE STRIP (K946321)Cornelia Damsky, Inc.1995-01-12
SPYROFLEX WOUND CLOSURES (K921775)Polymint Industrial Co. , Ltd.1992-05-19
AWC BUTTERFLY WOUND CLOSURES (K894802)American White Cross, Inc.1990-01-31
TECNOL SILK STRIP (K894205)Tecnol New Jersey Wound Care, Inc.1989-07-25
OMED WOUND CLOSURE STRIPS (K874813)Oxboro Medical Intl., Inc.1988-01-29
SKIN CLOSURE (K840945)Gainor Medical1984-10-31
SUTURE STRIP (K842621)Genetic Laboratories, Inc.1984-10-25
SKIN TECH. SURGI-STRIPS (K833258)Lee Tec Corp.1984-01-25
DERMA STRIP-TM SKIN CLOSURES (K833083)Howmedica Corp.1983-12-30

Recalls involving this device

No recalls on record reference this clearance.