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510(k) Data Aggregation
K Number
K964452Device Name
HEMATACHEK
Manufacturer
RICHMOND DIAGNOSTICS, INC.
Date Cleared
1997-02-20
(106 days)
Product Code
GLK
Regulation Number
864.8625Why did this record match?
Applicant Name (Manufacturer) :
RICHMOND DIAGNOSTICS, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Device Description
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