FDA 510(k) Applications Submitted by VYGON S A

FDA 510(k) Number Submission Date Device Name Applicant
K040657 03/12/2004 BOUSSIGNAC/VYGON ENDOTRACHEAL TUBE, MODEL 6501.25/30/35 AND 6502.70/75/80 VYGON S A
K013884 11/23/2001 BOUSSIGNAC C.P.A.P. DEVICE VYGON S A


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