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510(k) Data Aggregation
K Number
K974493Device Name
FIEGERT ENDOTECH FLEXIBLE FIBEROPTIC ENDOSCOPES, FIEGERT ENDOTECH FLEXIBLE VIDEO-ENDOSCOPES
Manufacturer
Date Cleared
1998-03-31
(123 days)
Regulation Number
876.1500Why did this record match?
Applicant Name (Manufacturer) :
FIEGERT-ENDOTECH MEDIZINTECHNIK GMBH
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Provide illumination to, and allow visual observation and/or surgical manipulation of body cavities, hollow organs and canals in the Gastrointestinal tract.
Device Description
Fiegert Endotech Flexible Fiberoptic Endoscopes; Fiegert Endotech Flexible Video-Endoscopes
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