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MYELOTEC VIDEO GUIDED CATHETER

Page Type
Cleared 510(K)
510(k) Number
K980734
510(k) Type
Traditional
Applicant
MYELOTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/1998
Days to Decision
167 days
Submission Type
Summary

MYELOTEC VIDEO GUIDED CATHETER

Page Type
Cleared 510(K)
510(k) Number
K980734
510(k) Type
Traditional
Applicant
MYELOTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/1998
Days to Decision
167 days
Submission Type
Summary