VEGA ULTRASONIC NEBULIZER


the company

Device Classification Name

nebulizer (direct patient interface)

510(k) Number K002831
Device Name VEGA ULTRASONIC NEBULIZER
Original Applicant
VEGA TECHNOLOGIES, INC.
11f-13, 100 chang-chun rd.
taipei, 

TW

104

Original Contact joseph lu
Regulation Number 868.5630
Classification Product Code
CAF  
Date Received 09/11/2000
Decision Date 05/23/2001
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Anesthesiology

510k Review Panel

Anesthesiology

Type Traditional
Reviewed by Third Party No

Combination Product

No