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510(k) Data Aggregation
K Number
K961316Device Name
WOUND HYDROGEL AND/OR STERILE WOUND HYDROGEL
Manufacturer
Date Cleared
1996-07-15
(101 days)
Product Code
Regulation Number
N/AWhy did this record match?
Applicant Name (Manufacturer) :
RENAISSANCE PHARMACEUTICAL, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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K Number
K961766Device Name
WOUND HYDROGEL & STERILE WOUND HYDROGEL
Manufacturer
Date Cleared
1996-07-15
(73 days)
Product Code
Regulation Number
N/AWhy did this record match?
Applicant Name (Manufacturer) :
RENAISSANCE PHARMACEUTICAL, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
Ask a Question
Ask a specific question about this device
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