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FIEGERT ENDOTECH FLEXIBLE FIBEROPTIC ENDOSCOPES, FIEGERT ENDOTECH FLEXIBLE VIDEO-ENDOSCOPES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974493
510(k) Type
Traditional
Applicant
FIEGERT-ENDOTECH MEDIZINTECHNIK GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/31/1998
Days to Decision
123 days
Submission Type
Statement

FIEGERT ENDOTECH FLEXIBLE FIBEROPTIC ENDOSCOPES, FIEGERT ENDOTECH FLEXIBLE VIDEO-ENDOSCOPES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974493
510(k) Type
Traditional
Applicant
FIEGERT-ENDOTECH MEDIZINTECHNIK GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/31/1998
Days to Decision
123 days
Submission Type
Statement