FDA 510(k) Application Details - K841810

Device Classification Name Syringe, Piston

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510(K) Number K841810
Device Name Syringe, Piston
Applicant MARTELL MEDICAL PRODUCTS, INC.

, US
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Regulation Number 880.5860

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Classification Product Code FMF
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Date Received 05/01/1984
Decision Date 07/06/1984
Decision SE - Substantially Equivalent
Classification Advisory Committee HO - General Hospital
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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