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FDA 510(k), K113066, CORVIS ST
FDA 510(k), K113066, CORVIS ST
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510(K) Number: K113066
Device Name: CORVIS ST
Manufacturer: OCULUS OPTIKGERATE GMBH
Device Classification Name: tonometer, ac-powered
Regulation Number: 886.1930
Classification Product Code: HKX
Date Received: 10/17/2011
Decision Date: 11/08/2012
Regulation Medical Specialty: Ophthalmic
Device Name: CORVIS ST
Manufacturer: OCULUS OPTIKGERATE GMBH
Device Classification Name: tonometer, ac-powered
Regulation Number: 886.1930
Classification Product Code: HKX
Date Received: 10/17/2011
Decision Date: 11/08/2012
Regulation Medical Specialty: Ophthalmic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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