FDA 510(k), K220606, Ambu aScope 5 Broncho HD 5.6/2.8, Ambu aScope 5 Broncho HD 5.0/2.2, Ambu aBox 2

510(K) Number: K220606
Device Name: Ambu aScope 5 Broncho HD 5.6/2.8, Ambu aScope 5 Broncho HD 5.0/2.2, Ambu aBox 2
Manufacturer: Gurpreet Kaur Rehal
Device Classification Name: Bronchoscope (Flexible Or Rigid)
Regulation Number: EOQ
Classification Product Code: 03/02/2022
Date Received: 07/25/2022
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Ear Nose & Throat