FDA.reportPublic FDA data

510(k) K771658

Device
IDENTOFLEX
Applicant
Cavitron Corp.
510(k) number
K771658
Product code
EHJ
Decision
Substantially Equivalent (SESE)
Decision date
1977-09-12
Date received
1977-08-30
Regulation
872.6010
Classification name
Disk, Abrasive
Medical specialty
Dental
Review panel
Dental
Device class
1
Clearance type
Traditional
Third party reviewed
N

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 EHJ#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K911111MICROMILLS, PATRIOTS, ALPHA GOLD DIAMONDSVermont Diamond Instruments1991-11-19
K873002MIN-IDENTOFLEXCentrix, Inc.1987-08-17
K790640HOWMEDICA BRASS CENTER DISCE.C. Moore Co.1979-05-01