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CARTER-THOMASON NEEDLE-POINT SUTURE PASSER INSTRUMENT SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980123
510(k) Type
Traditional
Applicant
LOUISVILLE LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/1998
Days to Decision
54 days
Submission Type
Statement