FDA.reportPublic FDA data

510(k) K770492

Device
CRACK DETECTOR, DEN-MAT
Applicant
Dey-Mat, Inc.
510(k) number
K770492
Product code
EFH
Decision
Substantially Equivalent (SESE)
Decision date
1977-03-21
Date received
1977-03-14
Regulation
872.6140
Classification name
Paper, Articulation
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 EFH#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K965026PFINGST PRESSURE PASTEPfingst & Co., Inc.1997-02-10
K912632OCCLUDEPascal Co., Inc.1992-01-17
K911259HYDENTPascal Co., Inc.1991-06-06
K864572FIXTECTORProdent Intl., Inc.1987-02-12
K870032REVISED T-SCAN SYSTEMSentek, Inc.1987-02-02
K832647ARTICULATING PAPERArdent Intl., Inc.1984-02-21
K833132MUCOSAL ADJUSTMENT PASTE LIQUID SPRAYMyo-Tronics Research, Inc.1984-02-10
K810498CENTRIC (BITE) REGISTRATION PASTEWallace A. Erickson & Co.1981-03-17
K771011ARTICULATING PAPERParker Laboratories, Inc.1977-06-20