TYMPANOSTOMY VENTILATION TUBE— 510(k) K961945

Name: FDA 510(k) clearance K961945
Creator: U.S. Food and Drug Administration
Published: 1996-06-11

Substantially Equivalent

Advanced Microbotics Corp.

FDA 510(k) clearance K961945 for TYMPANOSTOMY VENTILATION TUBE, Substantially Equivalent on 1996-06-11. Applicant: Advanced Microbotics Corp.. Device class: 2.

Clearance details

Applicant: Advanced Microbotics Corp.
Product code: Code ETD
Device class: Class 2
Regulation: 21 CFR 874.3880
Advisory panel: Ear, Nose, Throat
Date received: 1996-05-20
Decision date: 1996-06-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Portland, OR, US

Download summary PDF View on FDA.gov ↗

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