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FDA 510(k) Application Details - K102222
Device Classification Name
Instrument, Vitreous Aspiration And Cutting, Ac-Powered
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510(K) Number
K102222
Device Name
Instrument, Vitreous Aspiration And Cutting, Ac-Powered
Applicant
MEDICAL INSTRUMENT DEVELOPMENT LABORATORIES, INC.
557 MC CORMICK STREET
SAN LEANDRO, CA 94577 US
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LINDA UPTON
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Regulation Number
886.4150
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Classification Product Code
HQE
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More FDA Info for this Product Code
Date Received
08/06/2010
Decision Date
04/08/2011
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OP - Ophthalmic
Review Advisory Committee
OP - Ophthalmic
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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