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FDA 510(k), K911109, OPHTA SIL (R), LACHRYMAL INTUBATION SETS
FDA 510(k), K911109, OPHTA SIL (R), LACHRYMAL INTUBATION SETS
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510(K) Number: K911109
Device Name: OPHTA SIL (R), LACHRYMAL INTUBATION SETS
Manufacturer: G.W.B. INTL., LTD.
Device Classification Name: lacrimal stents and intubation sets
Regulation Number:
Classification Product Code: OKS
Date Received: 03/04/1991
Decision Date: 05/01/1991
Regulation Medical Specialty:
Device Name: OPHTA SIL (R), LACHRYMAL INTUBATION SETS
Manufacturer: G.W.B. INTL., LTD.
Device Classification Name: lacrimal stents and intubation sets
Regulation Number:
Classification Product Code: OKS
Date Received: 03/04/1991
Decision Date: 05/01/1991
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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