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VAGINAL SUTURING KIT FOR LAPAROTOMY BLADDER NECK SUSPENSION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971791
510(k) Type
Traditional
Applicant
Louisville Laboratories, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1997
Days to Decision
76 days
Submission Type
Summary

VAGINAL SUTURING KIT FOR LAPAROTOMY BLADDER NECK SUSPENSION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971791
510(k) Type
Traditional
Applicant
Louisville Laboratories, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1997
Days to Decision
76 days
Submission Type
Summary