FDA 510(k), K984443, ORBSCAN
FDA 510(k), K984443, ORBSCAN
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$149.00 USD
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510(K) Number: K984443
Device Name: ORBSCAN
Manufacturer:
Device Classification Name: Device, Analysis, Anterior Segment
Regulation Number: 886.1850
Classification Product Code: MXK
Date Received: 12/14/1998
Decision Date: 03/05/1999
Regulation Medical Specialty: Ophthalmic
Device Name: ORBSCAN
Manufacturer:
Device Classification Name: Device, Analysis, Anterior Segment
Regulation Number: 886.1850
Classification Product Code: MXK
Date Received: 12/14/1998
Decision Date: 03/05/1999
Regulation Medical Specialty: Ophthalmic