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FDA 510(k), K896622, VISITEC VITRECTOMY UNIT
FDA 510(k), K896622, VISITEC VITRECTOMY UNIT
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510(K) Number: K896622
Device Name: VISITEC VITRECTOMY UNIT
Manufacturer: VISITEC CO.
Device Classification Name: Instrument, Vitreous Aspiration And Cutting, Battery-Powered
Regulation Number: 886.4150
Classification Product Code: HKP
Date Received: 11/21/1989
Decision Date: 04/04/1990
Regulation Medical Specialty: Ophthalmic
Device Name: VISITEC VITRECTOMY UNIT
Manufacturer: VISITEC CO.
Device Classification Name: Instrument, Vitreous Aspiration And Cutting, Battery-Powered
Regulation Number: 886.4150
Classification Product Code: HKP
Date Received: 11/21/1989
Decision Date: 04/04/1990
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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