Last synced on 14 November 2025 at 11:06 pm

ESTECH PERCUTANEOUS INSERTION DILATOR KIT

Page Type
Cleared 510(K)
510(k) Number
K070749
510(k) Type
Traditional
Applicant
Coombs Medical Device Consulting
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2007
Days to Decision
219 days
Submission Type
Summary

ESTECH PERCUTANEOUS INSERTION DILATOR KIT

Page Type
Cleared 510(K)
510(k) Number
K070749
510(k) Type
Traditional
Applicant
Coombs Medical Device Consulting
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2007
Days to Decision
219 days
Submission Type
Summary