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AUTO SUTURE LAPAROSCOPIC FASCIA CLOSURE DEVICE II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
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510(k) Number
K940398
510(k) Type
Traditional
Applicant
UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
4/7/1994
Days to Decision
70 days
Submission Type
Summary