FDA.reportPublic FDA data

510(k) K810888

Device
Boundary Tubing Holders
Applicant
THE BUCKEYE CELLULOSE CORP.
510(k) number
K810888
Product code
FZX
Decision
Substantially Equivalent (SESE)
Decision date
1981-04-23
Date received
1981-04-02
Regulation
878.4800
Classification name
Guide, Surgical, Instrument
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 FZX#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K914715PARALLELING GUIDESImplant Corp. of America1994-02-16
K871413CIVCO STEPPERCIVCO Medical Instruments Co., Inc.1987-07-14
K871503BIOPSY NEEDLE GUIDE KIT, STERILEAmedic USA1987-07-10
K862564A.C.L. GUIDE KITAspen Laboratories, Inc.1986-08-18
K854262MEADOX SURGIMED BREAST LOCALIZATION WIRE SET/ONLYMeadox Surgimed, Inc.1985-12-24
K852402NAMIC HOMER MAMMALOK NEEDLE/WIRE LOCALIZERNorth American Instrument Corp.1985-07-11
K842698BRITISH SPINAL FUSION SETDowns Surgical , Ltd.1984-09-12
K841618THREADING TUBEPlastafil, Inc.1984-08-27
K841619DRILL GUIDEPlastafil, Inc.1984-07-11
K841297TECHMEDICA DRILL GUIDETechmedica, Inc.1984-04-25
K840835STRAITH DRAIN INSERTERSurgical Technology Laboratories, Inc.1984-04-23
K834350ACUFEX DREZ COMMUNICATING DRILL GUIDEAcufex Microsurgical, Inc.1984-03-19
K830720GRAF MENISCAL SUTURE SETAcufex Microsurgical, Inc.1983-06-16
K821618DISPOSABLE NEEDLE HOLDERSMedcare Products1982-06-21
K810788SURGICAL TUBE HOLDERThe Urology Group1981-04-17