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FDA 510(k) Applications Submitted by FIDIA PHARMACEUTICAL CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K963004
08/02/1996
BIONECT CREAM
FIDIA PHARMACEUTICAL CORP.
K973722
09/30/1997
BIONECT HYDROGEL FOAM
FIDIA PHARMACEUTICAL CORP.
K973724
09/30/1997
BIONECT HYDROGEL SPRAY
FIDIA PHARMACEUTICAL CORP.
K973725
09/30/1997
BIONECT CLEAR HYDROGEL
FIDIA PHARMACEUTICAL CORP.
K984262
11/17/1998
MODIFICATION OF BIONECT HYDROGEL GAUZE PADS
FIDIA PHARMACEUTICAL CORP.
K984264
11/17/1998
MODIFICATION OF BIONECT CLEAR HYDROGEL
FIDIA PHARMACEUTICAL CORP.
K984266
11/17/1998
MODIFICATION OF BIONECT HYDROGEL SPRAY
FIDIA PHARMACEUTICAL CORP.
K984267
11/17/1998
MODIFICATION OF BIONECT HYDROGEL FOAM
FIDIA PHARMACEUTICAL CORP.
K984413
11/17/1998
BIONECT HYDROGEL
FIDIA PHARMACEUTICAL CORP.
K973721
09/30/1997
BIONECT HYDROGEL GAUZE PADS
FIDIA PHARMACEUTICAL CORP.
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