FDA 510(k) Application Details - K833387

Device Classification Name

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510(K) Number K833387
Device Name ARGON LASER SURGICAL SYSTEM 770
Applicant COOPER MEDICAL CORP.

, US
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Regulation Number

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Classification Product Code ZZZ
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Date Received 09/29/1983
Decision Date 04/18/1984
Decision SE - Substantially Equivalent
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee -
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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