DIXIE USA PTL, PHARYNGEAL TRACHEAL LUMEN— 510(k) K831481

Name: FDA 510(k) clearance K831481
Creator: U.S. Food and Drug Administration
Published: 1983-10-04

Substantially Equivalent

Eugene Scarberry

FDA 510(k) clearance K831481 for DIXIE USA PTL, PHARYNGEAL TRACHEAL LUMEN, Substantially Equivalent on 1983-10-04. Applicant: Eugene Scarberry. Device class: 2.

Clearance details

Applicant: Eugene Scarberry
Product code: Code DSK
Device class: Class 2
Regulation: 21 CFR 870.1110
Advisory panel: Cardiovascular
Date received: 1983-05-09
Decision date: 1983-10-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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