MAX-I-PROBE PERIODONTAL ENDODONTIC PROB— 510(k) K840237

Name: FDA 510(k) clearance K840237
Creator: U.S. Food and Drug Administration
Published: 1984-04-05

Substantially Equivalent

Smith & Nephew, Mpl Division

FDA 510(k) clearance K840237 for MAX-I-PROBE PERIODONTAL ENDODONTIC PROB, Substantially Equivalent on 1984-04-05. Applicant: Smith & Nephew, Mpl Division. Device class: 1.

Clearance details

Applicant: Smith & Nephew, Mpl Division
Product code: Code EIC
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1984-01-20
Decision date: 1984-04-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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