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MYELOTEC MYELOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K960194
510(k) Type
Traditional
Applicant
MYELOTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1996
Days to Decision
232 days
Submission Type
Summary

MYELOTEC MYELOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K960194
510(k) Type
Traditional
Applicant
MYELOTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1996
Days to Decision
232 days
Submission Type
Summary