3M Disposable Skin Stapler

FDA 510(k) K800535 · 3M Company

Substantially Equivalent

510(k) numberK800535

Submission

Device name
3M Disposable Skin Stapler
Applicant
3M Company
White City, OR, US
Received
March 10, 1980
Decision date
April 4, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GDT – Staple, Removable (Skin)
Device class
Class I (low risk)
Regulation
21 CFR 878.4760
Specialty
General, Plastic Surgery

Other 510(k)s with product code GDT

510(k)DeviceApplicantDecision
K963234Staple Removal KitGDT · Traditional Continental Medical Laboratories, Inc.10/21/1996SE
K943719Visistat StaplerGDT · Traditional Pilling Weck, Inc.08/24/1994SE
K925526Manipler Disposable Skin StaplerGDT · Traditional Matsutani Seisakusho Co. , Ltd.06/24/1993SE
K915430Skin Staple Remover KitGDT · Traditional Cypress Medical Products, Ltd.02/28/1992SEKD
K911204Qualtex Skin Staple ExtractorGDT · Traditional Deroyal Industries, Inc.05/08/1991SE
K910586Auto Suture(R) Polymer Skin Graft Stapler*GDT · Traditional United States Surgical, A Division of Tyco Healthc03/07/1991SE
K900486Appose Unity Sterile Disposable Skin StaplerGDT · Traditional Davis & Geck, Inc.04/20/1990SE
K861711Skin Staple Remover with Sponge Sterile DisposableGDT · Traditional Busse Hospital Disposables, Inc.05/16/1986SE
K851974V. Mueller Vital Skin StaplerGDT · Traditional American V. Mueller06/11/1985SE
K844838Skin Stat II Skin Stapling Medical DeviceGDT · Traditional Edward Weck, Inc.01/23/1985SE

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Questions and answers

When was 3M Disposable Skin Stapler cleared by the FDA?

3M Disposable Skin Stapler (K800535) received a 510(k) decision of Substantially Equivalent on April 4, 1980, 25 days after the submission was received.

What is the product code of K800535?

The FDA product code is GDT – Staple, Removable (Skin), a Class I (low risk) device regulated under 21 CFR 878.4760.