Last synced on 20 December 2024 at 11:05 pm

E.R.C.P. CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914495
510(k) Type
Traditional
Applicant
SURGITEK MEDICAL ENGINEERING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1992
Days to Decision
114 days
Submission Type
Summary

E.R.C.P. CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914495
510(k) Type
Traditional
Applicant
SURGITEK MEDICAL ENGINEERING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1992
Days to Decision
114 days
Submission Type
Summary