FDA.reportPublic FDA data

510(k) K760734

Device
Regular And Wide Skin Staples
Applicant
ETHICON, INC.
510(k) number
K760734
Product code
GDT
Decision
Substantially Equivalent (SESE)
Decision date
1976-11-03
Date received
1976-09-28
Regulation
878.4760
Classification name
Staple, Removable (Skin)
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code GDT#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K963234STAPLE REMOVAL KITContinental Medical Laboratories, Inc.1996-10-21
K943719VISISTAT STAPLERPilling Weck, Inc.1994-08-24
K925526MANIPLER DISPOSABLE SKIN STAPLERMatsutani Seisakusho Co. , Ltd.1993-06-24
K915430SKIN STAPLE REMOVER KITCypress Medical Products, Ltd.1992-02-28
K911204QUALTEX SKIN STAPLE EXTRACTORDeroyal Industries, Inc.1991-05-08
K910586AUTO SUTURE(R) POLYMER SKIN GRAFT STAPLER*United States Surgical, A Division of Tyco Healthc1991-03-07
K900486APPOSE UNITY STERILE DISPOSABLE SKIN STAPLERDavis & Geck, Inc.1990-04-20
K861711SKIN STAPLE REMOVER WITH SPONGE STERILE DISPOSABLEBusse Hospital Disposables, Inc.1986-05-16
K851974V. MUELLER VITAL SKIN STAPLERAmerican V. Mueller1985-06-11
K844838SKIN STAT II SKIN STAPLING MEDICAL DEVICEEdward Weck, Inc.1985-01-23
K844837VISISTAT SKIN STAPLING DEVICEEdward Weck, Inc.1985-01-23
K833085STAPLE REMOVER SR300PProsper, Inc.1984-12-14
K833357VYDAX 525-550 & 5100 FLUOROTELOMERETHICON, Inc.1983-12-12
K832709SKIN STAPLING DEVICE SC2000Prosper, Inc.1983-09-26
K822365CENTURION SKIN STAPLE REMOVERTri-State1982-08-27