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FDA 510(k), K061404, MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICE
FDA 510(k), K061404, MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICE
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510(K) Number: K061404
Device Name: MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICE
Manufacturer: FCI OPHTHALMICS, INC.
Device Classification Name: lacrimal stents and intubation sets
Regulation Number:
Classification Product Code: OKS
Date Received: 05/19/2006
Decision Date: 08/07/2006
Regulation Medical Specialty:
Device Name: MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICE
Manufacturer: FCI OPHTHALMICS, INC.
Device Classification Name: lacrimal stents and intubation sets
Regulation Number:
Classification Product Code: OKS
Date Received: 05/19/2006
Decision Date: 08/07/2006
Regulation Medical Specialty:
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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