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510(k) Data Aggregation
K Number
K970827Device Name
PRECISE
Manufacturer
Date Cleared
1997-04-16
(41 days)
Product Code
Regulation Number
872.3710Why did this record match?
Applicant Name (Manufacturer) :
ALLAN SCHULMAN,D.D.S., M.S.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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