FDA 510(k), K121959, EVIS EXERA III VIDEO SYSTEM
FDA 510(k), K121959, EVIS EXERA III VIDEO SYSTEM
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510(K) Number: K121959
Device Name: EVIS EXERA III VIDEO SYSTEM
Manufacturer:
Device Classification Name: Bronchoscope (Flexible Or Rigid)
Regulation Number: 874.4680
Classification Product Code: EOQ
Date Received: 07/05/2012
Decision Date: 01/10/2013
Regulation Medical Specialty: Ear Nose & Throat
Device Name: EVIS EXERA III VIDEO SYSTEM
Manufacturer:
Device Classification Name: Bronchoscope (Flexible Or Rigid)
Regulation Number: 874.4680
Classification Product Code: EOQ
Date Received: 07/05/2012
Decision Date: 01/10/2013
Regulation Medical Specialty: Ear Nose & Throat