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FDA 510(k), K200567, ASI Plethysmogrpah Analyzer
FDA 510(k), K200567, ASI Plethysmogrpah Analyzer
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510(K) Number: K200567
Device Name: ASI Plethysmogrpah Analyzer
Manufacturer: Arterial Stiffness Inc.
Device Classification Name: Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
Regulation Number: 870.2780
Classification Product Code: JOM
Date Received: 03/04/2020
Decision Date: 02/26/2021
Regulation Medical Specialty: Cardiovascular
Total Pages: 975
Fully Redacted Pages: 519
Content Pages: 456
Device Name: ASI Plethysmogrpah Analyzer
Manufacturer: Arterial Stiffness Inc.
Device Classification Name: Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
Regulation Number: 870.2780
Classification Product Code: JOM
Date Received: 03/04/2020
Decision Date: 02/26/2021
Regulation Medical Specialty: Cardiovascular
Total Pages: 975
Fully Redacted Pages: 519
Content Pages: 456
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