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BIONECT HYDROGEL FOAM

Page Type
Cleared 510(K)
510(k) Number
K973722
510(k) Type
Traditional
Applicant
FIDIA PHARMACEUTICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/1998
Days to Decision
357 days
Submission Type
Summary

BIONECT HYDROGEL FOAM

Page Type
Cleared 510(K)
510(k) Number
K973722
510(k) Type
Traditional
Applicant
FIDIA PHARMACEUTICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/1998
Days to Decision
357 days
Submission Type
Summary