Florida Probe Periodontal Probe

FDA 510(k) K890493 · Florida Probe Corp.

Substantially Equivalent

510(k) numberK890493

Submission

Device name
Florida Probe Periodontal Probe
Applicant
Florida Probe Corp.
Gainesville, FL, US
Received
January 31, 1989
Decision date
March 13, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
EIL – Gauge, Depth, Instrument, Dental
Device class
Class I (low risk)
Regulation
21 CFR 872.4565
Specialty
Dental

Other 510(k)s with product code EIL

510(k)DeviceApplicantDecision
K911643Abiodent Periotemp(R) SystemEIL · Traditional Abiomed, Inc.07/09/1991SE
K885075Abiomed Periotemp(Tm) ProbeEIL · Traditional Abiomed, Inc.02/13/1989SE
K884813Model 200A Electronic Force-Sensing ProbeEIL · Traditional Vine Valley Research01/05/1989SE
K880209Periodontal Probe - AutoprobeEIL · Traditional Dentsply Intl.04/27/1988SE
K872098Cremeen Alveolar Bone CaliperEIL · Traditional Bowen & Company, Inc.07/31/1987SE
K872215Perio-TestEIL · Traditional Dr. Bernard Loewenthal07/10/1987SE
K822793Pio Root Canal IndicatorEIL · Traditional National Patent Development Corp.10/22/1982SE

More from National Patent Development Corp.

510(k)DeviceDecision
K875076Florida ProbeEIX · Traditional 03/10/1988SE

Questions and answers

When was Florida Probe Periodontal Probe cleared by the FDA?

Florida Probe Periodontal Probe (K890493) received a 510(k) decision of Substantially Equivalent on March 13, 1989, 41 days after the submission was received.

What is the product code of K890493?

The FDA product code is EIL – Gauge, Depth, Instrument, Dental, a Class I (low risk) device regulated under 21 CFR 872.4565.