FDA 510(k) Application Details - K770102

Device Classification Name Forceps, Ophthalmic

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510(K) Number K770102
Device Name Forceps, Ophthalmic
Applicant EDWARD WECK, INC.

, US
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Regulation Number 886.4350

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Classification Product Code HNR
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Date Received 01/17/1977
Decision Date 01/24/1977
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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