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510(k) K801887

Device
DRILL, DENTAL
Applicant
AESCULAP INSTRUMENTS CORP.
510(k) number
K801887
Product code
DZA  
Decision
Substantially Equivalent (SESE)
Decision date
1980-08-20
Date received
1980-07-28
Regulation
872.4130
Classification name
Drill, Dental, Intraoral
Medical specialty
Dental
Review panel
Dental
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 DZA  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K984508SURGICAL CONTRA-ANGLE HANDPIECES, MODELS 975 AE,979 E/KM, 985 AE, 986 AE, 988 E/KM AND SURGICAL STRAIGHT HANDPIECES MODW&H Dentalwerk Buermoos GmbH1999-06-25
K962979S-53 INTRORAL DENTAL SYSTEMDel Medical Systems Corp.1996-09-25
K954790PROFILE NICKEL TITANIUM ROTARY INSTRUMENTSTulsa Dental Products, Ltd.1996-01-16
K914724ADA SHANK EXTENSIONImplant Corp. of America1993-07-27
K905418GATES GLIDDEN DRILLSThe Hygenic Corp.1991-07-25
K901097FILLOCK REAMERIvoclar North America, Inc.1990-04-25
K896149ANEST-EZE DENTAL DRILL RA#2Signature One Products, Inc.1990-01-19
K884187INDENTEC DRILL RA #1Phillip C. Crawford, D.D.S.1988-12-22
K811113RIESS-LUHRAllomedic1981-06-16
K801888HANDPIECE, DENTALAesculap Instruments Corp.1980-08-20
K761275AIROTOS LF HANDPIECEDentsply Intl.1976-12-23
K760956SURGICAL MICRO DRILLAmerican Safety Equipment Corp.1976-11-19

Legacy Summary#

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FDA Review#

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