FDA 510(k), K942533, NOVALENS/NOVAWET PERCEPTION AND VANGUARD

FDA 510(k), K942533, NOVALENS/NOVAWET PERCEPTION AND VANGUARD

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510(K) Number: K942533
Device Name: NOVALENS/NOVAWET PERCEPTION AND VANGUARD
Manufacturer:
Device Classification Name: Lens, Contact (Other Material) - Daily
Regulation Number: 886.5916
Classification Product Code: HQD
Date Received: 05/27/1994
Decision Date: 08/05/1994
Regulation Medical Specialty: Ophthalmic
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