Last synced on 19 July 2024 at 11:05 pm

SUPERSTITCH VASCULAR SUTURING DEVICE, 6 FRENCH, MODELS 06-15-00X; MID-LENGTH 06-25-00X

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020940
510(k) Type
Special
Applicant
SUTURA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2002
Days to Decision
26 days
Submission Type
Summary

SUPERSTITCH VASCULAR SUTURING DEVICE, 6 FRENCH, MODELS 06-15-00X; MID-LENGTH 06-25-00X

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020940
510(k) Type
Special
Applicant
SUTURA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2002
Days to Decision
26 days
Submission Type
Summary