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BIONECT HYDROGEL

Page Type
Cleared 510(K)
510(k) Number
K984413
510(k) Type
Traditional
Applicant
FIDIA PHARMACEUTICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1999
Days to Decision
85 days
Submission Type
Summary

BIONECT HYDROGEL

Page Type
Cleared 510(K)
510(k) Number
K984413
510(k) Type
Traditional
Applicant
FIDIA PHARMACEUTICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1999
Days to Decision
85 days
Submission Type
Summary