The following data is part of a premarket notification filed by Florida Probe Corp. with the FDA for Florida Probe Periodontal Probe.
| Device ID | K890493 |
| 510k Number | K890493 |
| Device Name: | FLORIDA PROBE PERIODONTAL PROBE |
| Classification | Gauge, Depth, Instrument, Dental |
| Applicant | FLORIDA PROBE CORP. 1820 N.E. 23RD AVE. Gainesville, FL 32609 |
| Contact | Gibbs, Phd |
| Correspondent | Gibbs, Phd FLORIDA PROBE CORP. 1820 N.E. 23RD AVE. Gainesville, FL 32609 |
| Product Code | EIL |
| CFR Regulation Number | 872.4565 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-01-31 |
| Decision Date | 1989-03-13 |