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ESTECH PERCUTANEOUS INSERTION DILATOR KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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