PULMOCATH INTRABRONCHIAL CATHETER— 510(k) K901615

Substantially Equivalent

Omnitron Intl., Inc.

FDA 510(k) clearance K901615 for PULMOCATH INTRABRONCHIAL CATHETER, Substantially Equivalent on 1992-11-27. Applicant: Omnitron Intl., Inc..

Clearance details

Applicant: Omnitron Intl., Inc.
Product code: Code JAQ
Advisory panel: Radiology
Date received: 1990-04-06
Decision date: 1992-11-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lajke Charles, LA, US

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