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FDA 510(k), K101182, IOLMASTER 500
FDA 510(k), K101182, IOLMASTER 500
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510(K) Number: K101182
Device Name: IOLMASTER 500
Manufacturer: CARL ZEISS MEDITEC AG
Device Classification Name: biomicroscope, slit-lamp, ac-powered
Regulation Number: 886.1850
Classification Product Code: HJO
Date Received: 04/27/2010
Decision Date: 11/03/2010
Regulation Medical Specialty: Ophthalmic
Device Name: IOLMASTER 500
Manufacturer: CARL ZEISS MEDITEC AG
Device Classification Name: biomicroscope, slit-lamp, ac-powered
Regulation Number: 886.1850
Classification Product Code: HJO
Date Received: 04/27/2010
Decision Date: 11/03/2010
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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