FDA 510(k) Application Details - K874336

Device Classification Name Perimeter, Automatic, Ac-Powered

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510(K) Number K874336
Device Name Perimeter, Automatic, Ac-Powered
Applicant LKC TECHNOLOGIES, INC.
2 PROFESSIONAL DR., SUITE 222
GAITHERSBURG, MD US
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Contact JEROME LEIGHT
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Regulation Number 886.1605

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Classification Product Code HPT
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Date Received 10/22/1987
Decision Date 01/12/1988
Decision SE - Substantially Equivalent
Classification Advisory Committee OP - Ophthalmic
Review Advisory Committee OP - Ophthalmic
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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