510(k) K872215

Device
Perio-test
Applicant
DR. BERNARD LOEWENTHAL
510(k) number
K872215
Product code
EIL
Decision
Substantially Equivalent (SESE)
Decision date
1987-07-10
Date received
1987-06-09
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
BERNARD LOEWENTHAL
Address
278 Lafayette Rd. Portsmouth NH US 03801 03801

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
K880209PERIODONTAL PROBE - AUTOPROBEDentsply Intl.1988-04-27
K872098CREMEEN ALVEOLAR BONE CALIPERBowen & Company, Inc.1987-07-31
K822793PIO ROOT CANAL INDICATORNational Patent Development Corp.1982-10-22