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FDA 510(k) Application Details - K972150
Device Classification Name
Bandage, Liquid
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510(K) Number
K972150
Device Name
Bandage, Liquid
Applicant
PROCYTE CORP.
P.O. BOX 808
REDMOND,, WA 98073-0808 US
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Contact
PAUL KETTERIDGE
Other 510(k) Applications for this Contact
Regulation Number
880.5090
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Classification Product Code
KMF
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More FDA Info for this Product Code
Date Received
06/09/1997
Decision Date
12/10/1997
Decision
SN - Substantially Equivalent for Some Indications
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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