FDA 510(k), K032104, AMNIOLENS

FDA 510(k), K032104, AMNIOLENS

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510(K) Number: K032104
Device Name: AMNIOLENS
Manufacturer:
Device Classification Name: Conformer, Ophthalmic, Biological Tissue
Regulation Number: 886.3130
Classification Product Code: NQB
Date Received: 07/08/2003
Decision Date: 12/12/2003
Regulation Medical Specialty: Ophthalmic
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