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FDA 510(k), K052674, CONTACT LENS OPHTHALMODYNAMOMETER
FDA 510(k), K052674, CONTACT LENS OPHTHALMODYNAMOMETER
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510(K) Number: K052674
Device Name: CONTACT LENS OPHTHALMODYNAMOMETER
Manufacturer: MEDITRON, GMBH
Device Classification Name: ophthalmodynamometer, diagnostic contact lens, polymethylmethacrylate (pmma)
Regulation Number: 886.1385
Classification Product Code: NYK
Date Received: 09/27/2005
Decision Date: 05/24/2006
Regulation Medical Specialty: Ophthalmic
Device Name: CONTACT LENS OPHTHALMODYNAMOMETER
Manufacturer: MEDITRON, GMBH
Device Classification Name: ophthalmodynamometer, diagnostic contact lens, polymethylmethacrylate (pmma)
Regulation Number: 886.1385
Classification Product Code: NYK
Date Received: 09/27/2005
Decision Date: 05/24/2006
Regulation Medical Specialty: Ophthalmic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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