DILATOR TUBE SET— 510(k) K120590

Substantially Equivalent

Koros USA, Inc.

FDA 510(k) clearance K120590 for DILATOR TUBE SET, Substantially Equivalent on 2013-05-07. Applicant: Koros USA, Inc..

Clearance details

Applicant: Koros USA, Inc.
Product code: Code PDQ
Advisory panel: Ear, Nose, Throat
Date received: 2012-02-28
Decision date: 2013-05-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Moorepark, CA, US

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