FDA 510(k) Applications Submitted by NEUROREGEN, L.L.C.

FDA 510(k) Applications Submitted by NEUROREGEN, L.L.C.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K983007	08/28/1998	NEUROTUBE	NEUROREGEN, L.L.C.

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