FDA 510(k), K030719, PENTACAM SCHEIMPFLUG CAMERA

FDA 510(k), K030719, PENTACAM SCHEIMPFLUG CAMERA

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510(K) Number: K030719
Device Name: PENTACAM SCHEIMPFLUG CAMERA
Manufacturer:
Device Classification Name: Device, Analysis, Anterior Segment
Regulation Number: 886.1850
Classification Product Code: MXK
Date Received: 03/07/2003
Decision Date: 09/16/2003
Regulation Medical Specialty: Ophthalmic
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