Last synced on 14 November 2025 at 11:06 pm

SMART DILATOR

Page Type
Cleared 510(K)
510(k) Number
K082995
510(k) Type
Traditional
Applicant
SAFESTITCH MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/6/2009
Days to Decision
121 days
Submission Type
Summary

SMART DILATOR

Page Type
Cleared 510(K)
510(k) Number
K082995
510(k) Type
Traditional
Applicant
SAFESTITCH MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/6/2009
Days to Decision
121 days
Submission Type
Summary