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LAPAROTOMY BLADDER NECK SUSPENSION KIT

Page Type
Cleared 510(K)
510(k) Number
K971801
510(k) Type
Traditional
Applicant
LOUISVILLE LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/1997
Days to Decision
68 days
Submission Type
Summary

LAPAROTOMY BLADDER NECK SUSPENSION KIT

Page Type
Cleared 510(K)
510(k) Number
K971801
510(k) Type
Traditional
Applicant
LOUISVILLE LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/1997
Days to Decision
68 days
Submission Type
Summary