FDA.reportPublic FDA data

510(k) K926205

Device
Monosteryl
Applicant
UTENSILI SUPER ABRASIVI
510(k) number
K926205
Product code
EJL
Decision
Substantially Equivalent (SESE)
Decision date
1994-02-10
Date received
1992-12-09
Regulation
872.3240
Classification name
Bur, Dental
Medical specialty
Dental
Review panel
Dental
Device class
1
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
SUSAN KNOX
Address
Via Donizetti, 10 20095 Cusano Milanino (Milan), Italy IT

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code EJL#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K080687SMARTBURSS.S. White Burs, Inc.2008-06-20
K071352CERADRILLGebr. Brasseler GmbH & Co. KG2007-06-29
K061383BTI STERILE DENTAL DRILLS KIT, BTI ABUTMENTS AND CAPSB.T.I. Biotechnology Institute, Sl.2006-08-03
K943273TRI HAWK BUR, FG BURTri Hawk Corp.1994-08-01
K923883DENTAL OR SURGICAL BURStratum Dental Technologies, Inc.1993-07-27
K921406SILICONT BUR BLOCKInnovators, Inc.1992-04-28
K920243SMART BURS TOTAL CARBIDESVermont Diamond Instruments1992-03-25
K911208TIN COATED DENTAL BURSSurgical Precision Instruments, Corp.1991-09-16
K910794SMALL INSTRUMENT STERILIZATION/BUR BOXBrevet, Inc.1991-05-23
K882183DENTAL BURSTri-Stage, Inc.1988-06-21
K873698STERILIZED DENTAL BIT PACKAGINGFlorida Diamond Instruments Corp.1987-12-03
K863097CB BURBeavers Dental, Div. Sybron Canada, Ltd.1986-08-26
K854690DIAMONDS BURS-COMPOSIT FINISHINGAlmore Intl., Inc.1986-03-25
K854691DIAMOND BURS-HANDPIECEAlmore Intl., Inc.1986-03-25
K842720BUR, DENTAL GUTTA PERCHA-FILE-PULP CANALPenn-Med Technology, Inc.1985-05-21