FDA 510(k) Applications Submitted by BIOSURGICAL CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K964597 11/18/1996 BIOSURGICAL, CORP. MULTI CHAMBER SUCTION SYRINGE BIOSURGICAL CORP.
K000048 01/07/2000 SEALOUETTE FIBRIN SEALANT EXTENDED DROPLET APPLICATOR, MODEL TE-1 BIOSURGICAL CORP.
K000438 02/10/2000 MULTI LUMEN SUCTION SYRINGE SPRAY DISPENSER BIOSURGICAL CORP.
K992351 07/14/1999 SEALOUETTE FIBRIN SEALANT APPLICATOR BIOSURGICAL CORP.


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