Op-Site Skin Closure Suture Adhesive

FDA 510(k) K801884 · Acme United Corp.

Substantially Equivalent

510(k) numberK801884

Submission

Device name
Op-Site Skin Closure Suture Adhesive
Applicant
Acme United Corp.
Mchenry, IL, US
Received
August 7, 1980
Decision date
October 10, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FPX – Strip, Adhesive, Closure, Skin
Device class
Class I (low risk)
Regulation
21 CFR 880.5240
Specialty
General Hospital

Other 510(k)s with product code FPX

510(k)DeviceApplicantDecision
K970441K-Klosure 2 Inch LENGTH/4 Inch LENGTH/8 Inch LENGTH/12 Inch LengthFPX · Traditional Medi-Flex Hospital Products, Inc.05/09/1997SE
K952947Delpore Skin ClosureFPX · Traditional Bitco Intl.07/24/1995SE
K952702Derma SealFPX · Traditional Ttl Medical06/28/1995SE
K946321Biostrip Sterile Wound Closure StripFPX · Traditional Cornelia Damsky, Inc.01/12/1995SE
K931005Dukal Skin Closure StripFPX · Traditional Dukal Corp.07/14/1993SE
K921775Spyroflex Wound ClosuresFPX · Traditional Polymint Industrial Co. , Ltd.05/19/1992SE
K894802Awc Butterfly Wound ClosuresFPX · Traditional American White Cross, Inc.01/31/1990SE
K894205Tecnol Silk StripFPX · Traditional Tecnol New Jersey Wound Care, Inc.07/25/1989SE
K874813Omed Wound Closure StripsFPX · Traditional Oxboro Medical Intl., Inc.01/29/1988SE
K840945Skin ClosureFPX · Traditional Gainor Medical10/31/1984SE

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K895764Modified Lyofoam Wound DressingsKMF · Traditional 09/10/1990SN
K871740Lyosheet Surgical Sheet for BurnsFPY · Traditional 06/09/1987SE
K864084Lyofoam C Odor-Absorbing DressingFRO · Traditional 11/21/1986SN
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K860818One Time Enteral Feeding BagKNT · Traditional 05/15/1986SE
K861015One Time Hyperal & Catheter Dressing Change TraysFOZ · Traditional 04/22/1986SE
K842186Acu-Derm Transparent Wound DressingNAD · Traditional 08/24/1984SE

Questions and answers

When was Op-Site Skin Closure Suture Adhesive cleared by the FDA?

Op-Site Skin Closure Suture Adhesive (K801884) received a 510(k) decision of Substantially Equivalent on October 10, 1980, 64 days after the submission was received.

What is the product code of K801884?

The FDA product code is FPX – Strip, Adhesive, Closure, Skin, a Class I (low risk) device regulated under 21 CFR 880.5240.