NEXUS INJECTION SITE (NIS), MODEL NIS-1


Device Classification Name

set, administration, intravascular

510(k) Number K024363
Device Name NEXUS INJECTION SITE (NIS), MODEL NIS-1
Original Applicant
NEXUS MEDICAL, LLC
11428 lostwood ln.
suite b
raleigh, 
NC 
27614

Original Contact jamie abourched
Regulation Number 880.5440
Classification Product Code
FPA  
Date Received 12/31/2002
Decision Date 02/19/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General Hospital

510k Review Panel

General Hospital

statement

statement

Type Traditional
Reviewed by Third Party No

Combination Product

No