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510(k) K873002

Device
MIN-IDENTOFLEX
Applicant
CENTRIX, INC.
510(k) number
K873002
Product code
EHJ  
Decision
Substantially Equivalent (SESE)
Decision date
1987-08-17
Date received
1987-08-04
Regulation
872.6010
Classification name
Disk, Abrasive
Medical specialty
Dental
Review panel
Dental
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
JOHN DISCKO
Address
30 Stran Rd. Milford CT US 06460 06460

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
K790640HOWMEDICA BRASS CENTER DISCE.C. Moore Co.1979-05-01
K771658IDENTOFLEXCavitron Corp.1977-09-12

Legacy Summary#

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FDA Review#

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