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MEDRAD FLEX INTERFACE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K971380
510(k) Type
Traditional
Applicant
MEDRAD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/1997
Days to Decision
80 days
Submission Type
Summary

MEDRAD FLEX INTERFACE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K971380
510(k) Type
Traditional
Applicant
MEDRAD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/1997
Days to Decision
80 days
Submission Type
Summary