FLORIDA PROBE
Probe, Periodontic
FLORIDA PROBE CORP.
The following data is part of a premarket notification filed by Florida Probe Corp. with the FDA for Florida Probe.
Pre-market Notification Details
| Device ID | K875076 |
| 510k Number | K875076 |
| Device Name: | FLORIDA PROBE |
| Classification | Probe, Periodontic |
| Applicant | FLORIDA PROBE CORP. 1918 S.W. 48TH AVE. Gainesville, FL 32608 |
| Contact | Charles H Gibbs,phd |
| Correspondent | Charles H Gibbs,phd FLORIDA PROBE CORP. 1918 S.W. 48TH AVE. Gainesville, FL 32608 |
| Product Code | EIX |
| CFR Regulation Number | 872.4565 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-12-09 |
| Decision Date | 1988-03-10 |
Trademark Results [FLORIDA PROBE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 FLORIDA PROBE 75109593 2128221 Live/Registered |
Florida Probe Corporation 1996-05-21 |
 FLORIDA PROBE 73705176 1588677 Dead/Cancelled |
FLORIDA PROBE CORPORATION 1988-01-11 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.