FDA 510(k) Application Details - K841492

Device Classification Name Extractor, Vacuum, Fetal

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510(K) Number K841492
Device Name Extractor, Vacuum, Fetal
Applicant MEDELA, INC.


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Regulation Number 884.4340

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Classification Product Code HDB
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Date Received 04/10/1984
Decision Date 05/07/1984
Decision SE - Substantially Equivalent
Classification Advisory Committee OB - Obstetrics/Gynecology
Review Advisory Committee OB - Obstetrics/Gynecology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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