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FLEX-NECK PD CATHETER, INFANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031351
510(k) Type
Traditional
Applicant
MEDIGROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2003
Days to Decision
141 days
Submission Type
Summary

FLEX-NECK PD CATHETER, INFANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031351
510(k) Type
Traditional
Applicant
MEDIGROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2003
Days to Decision
141 days
Submission Type
Summary