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510(k) Data Aggregation
K Number
K982617Device Name
TRACER
Manufacturer
Date Cleared
1999-04-09
(256 days)
Regulation Number
870.2800Why did this record match?
Applicant Name (Manufacturer) :
HEARTLAND MEDICAL SYSTEMS, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
PATICATS WIS TARY BE EXCERIENCING For હર CARDIAC EVENTS SymfromMic Purse RATE ABACAITAL
Device Description
TRACER
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