FLORIDA PROBE PERIODONTAL PROBE— 510(k) K890493

Name: FDA 510(k) clearance K890493
Creator: U.S. Food and Drug Administration
Published: 1989-03-13

Substantially Equivalent

Florida Probe Corp.

FDA 510(k) clearance K890493 for FLORIDA PROBE PERIODONTAL PROBE, Substantially Equivalent on 1989-03-13. Applicant: Florida Probe Corp.. Device class: 1.

Clearance details

Applicant: Florida Probe Corp.
Product code: Code EIL
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1989-01-31
Decision date: 1989-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gainesville, FL, US

Download summary PDF View on FDA.gov ↗

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