CLARUS MODEL 2240 SEMI-RIGID OTOSCOPE— 510(k) K932259

Name: FDA 510(k) clearance K932259
Creator: U.S. Food and Drug Administration
Published: 1993-12-15

Substantially Equivalent

Clarus Medical Systems, Inc.

FDA 510(k) clearance K932259 for CLARUS MODEL 2240 SEMI-RIGID OTOSCOPE, Substantially Equivalent on 1993-12-15. Applicant: Clarus Medical Systems, Inc.. Device class: 1.

Clearance details

Applicant: Clarus Medical Systems, Inc.
Product code: Code ERA
Device class: Class 1
Regulation: 21 CFR 874.4770
Advisory panel: Ear, Nose, Throat
Date received: 1993-04-20
Decision date: 1993-12-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

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