FDA 510(k) Applications Submitted by ROBERTO FIORENTINI

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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact