FDA 510(k) Application Details - K873809

Device Classification Name Unit, Electrosurgical Andcoagulation, With Accessories

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510(K) Number K873809
Device Name Unit, Electrosurgical Andcoagulation, With Accessories
Applicant ZIMMER ASPEN LABS
P.O. BOX 3936
ENGLEWOOD, CO US
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Contact JANE JOHNSON
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Regulation Number 878.4400

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Classification Product Code BWA
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Date Received 09/18/1987
Decision Date 11/20/1987
Decision SE - Substantially Equivalent
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee SU - General & Plastic Surgery
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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