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SUTURE PLACEMENT DEVICE AND ACCESSORIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981531
510(k) Type
Traditional
Applicant
LSI SOLUTIONS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/1998
Days to Decision
75 days
Submission Type
Summary