510(k) K880209

Device
Periodontal Probe - Autoprobe
Applicant
DENTSPLY INTL.
510(k) number
K880209
Product code
EIL
Decision
Substantially Equivalent (SESE)
Decision date
1988-04-27
Date received
1988-01-15
Regulation
872.4565
Classification name
Gauge, Depth, Instrument, Dental
Medical specialty
Dental
Review panel
Dental
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
JOHN O SEMMELMAN
Address
570 W. College Ave. P.O. Box 872 York PA US 17405 17405

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code EIL#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K911643ABIODENT PERIOTEMP(R) SYSTEMAbiomed, Inc.1991-07-09
K890493FLORIDA PROBE PERIODONTAL PROBEFlorida Probe Corp.1989-03-13
K885075ABIOMED PERIOTEMP(TM) PROBEAbiomed, Inc.1989-02-13
K884813MODEL 200A ELECTRONIC FORCE-SENSING PROBEVine Valley Research1989-01-05
K872098CREMEEN ALVEOLAR BONE CALIPERBowen & Company, Inc.1987-07-31
K872215PERIO-TESTDr. Bernard Loewenthal1987-07-10
K822793PIO ROOT CANAL INDICATORNational Patent Development Corp.1982-10-22