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SUTURE PLACEMENT DEVICE AND ACCESSORIES, FLEXIBLE SUTURE PLACEMENT DEVICE AND ACCESSORIES, LSI R SERIES SUTURE PLACEME

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100593
510(k) Type
Traditional
Applicant
LSI SOLUTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/13/2010
Days to Decision
225 days
Submission Type
Summary

SUTURE PLACEMENT DEVICE AND ACCESSORIES, FLEXIBLE SUTURE PLACEMENT DEVICE AND ACCESSORIES, LSI R SERIES SUTURE PLACEME

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100593
510(k) Type
Traditional
Applicant
LSI SOLUTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/13/2010
Days to Decision
225 days
Submission Type
Summary