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LS SERIES 200 FLOVISION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971981
510(k) Type
Traditional
Applicant
Systam
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/1998
Days to Decision
572 days
Submission Type
Summary

LS SERIES 200 FLOVISION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971981
510(k) Type
Traditional
Applicant
Systam
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/1998
Days to Decision
572 days
Submission Type
Summary