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GENIE CUP INTEGRATED SCREENING DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980836
510(k) Type
Traditional
Applicant
Applied Technology Ventures, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/1998
Days to Decision
117 days
Submission Type
Statement

GENIE CUP INTEGRATED SCREENING DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980836
510(k) Type
Traditional
Applicant
Applied Technology Ventures, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/1998
Days to Decision
117 days
Submission Type
Statement