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LD2000 SERIES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980565
510(k) Type
Traditional
Applicant
General Scanning, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/1998
Days to Decision
34 days
Submission Type
Summary

LD2000 SERIES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980565
510(k) Type
Traditional
Applicant
General Scanning, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/1998
Days to Decision
34 days
Submission Type
Summary