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FDA 510(k), K801969, ASNIS GUIDED SCREW SYSTEMS
FDA 510(k), K801969, ASNIS GUIDED SCREW SYSTEMS
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$49.00 USD
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$49.00 USD
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510(K) Number: K801969
Device Name: ASNIS GUIDED SCREW SYSTEMS
Manufacturer:
Device Classification Name: Specula, Ophthalmic
Regulation Number: HNC
Classification Product Code: KXA
Date Received: 08/19/1980
Decision Date: 08/27/1980
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Ophthalmic
Device Name: ASNIS GUIDED SCREW SYSTEMS
Manufacturer:
Device Classification Name: Specula, Ophthalmic
Regulation Number: HNC
Classification Product Code: KXA
Date Received: 08/19/1980
Decision Date: 08/27/1980
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Ophthalmic
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