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FDA 510(k), K071473, MODIFICATION TO SUPERDIMENSION/BRONCHUS PREMIUM 2
FDA 510(k), K071473, MODIFICATION TO SUPERDIMENSION/BRONCHUS PREMIUM 2
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$149.00 USD
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$149.00 USD
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510(K) Number: K071473
Device Name: MODIFICATION TO SUPERDIMENSION/BRONCHUS PREMIUM 2
Manufacturer:
Device Classification Name: Bronchoscope (Flexible Or Rigid)
Regulation Number: 874.4680
Classification Product Code: EOQ
Date Received: 05/29/2007
Decision Date: 07/12/2007
Regulation Medical Specialty: Ear Nose & Throat
Device Name: MODIFICATION TO SUPERDIMENSION/BRONCHUS PREMIUM 2
Manufacturer:
Device Classification Name: Bronchoscope (Flexible Or Rigid)
Regulation Number: 874.4680
Classification Product Code: EOQ
Date Received: 05/29/2007
Decision Date: 07/12/2007
Regulation Medical Specialty: Ear Nose & Throat
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