Atlas FDA

DERMA SEAL

FDA 510(k) clearance K952702 · decided 1995-06-28

Clearance details

K-number
K952702
Device name
DERMA SEAL
Applicant
Ttl Medical
Decision
Substantially Equivalent
Date received
1995-06-13
Decision date
1995-06-28
Days to decision
15 days
Clearance type
Traditional
Product code
FPX
Device class
1
Regulation number
880.5240
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Knoxville, TN, 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
BIOSTRIP STERILE WOUND CLOSURE STRIP (K946321)Cornelia Damsky, Inc.1995-01-12
DUKAL SKIN CLOSURE STRIP (K931005)Dukal Corp.1993-07-14
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.