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FDA 510(k) Application Details - K960393
Device Classification Name
Dressing, Wound And Burn, Occlusive
More FDA Info for this Device
510(K) Number
K960393
Device Name
Dressing, Wound And Burn, Occlusive
Applicant
EUROMED A/S
49 PLAIN ST.
NORTH ATTLEBORO, MA 02760 US
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Contact
DIANE E MINEAR
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Regulation Number
000.0000
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Classification Product Code
MGP
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More FDA Info for this Product Code
Date Received
01/29/1996
Decision Date
03/01/1996
Decision
SN - Substantially Equivalent for Some Indications
Classification Advisory Committee
-
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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