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FDA 510(k), K864959, OBF MODEL 112 VACUUM CUP SYSTEM
FDA 510(k), K864959, OBF MODEL 112 VACUUM CUP SYSTEM
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510(K) Number: K864959
Device Name: OBF MODEL 112 VACUUM CUP SYSTEM
Manufacturer: OCULAR BLOOD FLOW LABORATORIES, INC.
Device Classification Name: tonometer, ac-powered
Regulation Number: 886.1930
Classification Product Code: HKX
Date Received: 12/18/1986
Decision Date: 02/12/1987
Regulation Medical Specialty: Ophthalmic
Device Name: OBF MODEL 112 VACUUM CUP SYSTEM
Manufacturer: OCULAR BLOOD FLOW LABORATORIES, INC.
Device Classification Name: tonometer, ac-powered
Regulation Number: 886.1930
Classification Product Code: HKX
Date Received: 12/18/1986
Decision Date: 02/12/1987
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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