A
·
B
·
C
·
D
·
E
·
F
·
G
·
H
·
I
·
J
·
K
·
L
·
M
·
N
·
O
·
P
·
Q
·
R
·
S
·
T
·
U
·
V
·
W
·
X
·
Y
·
Z
·
OTHER
·

Directory Results for 510(k) SUMMARY DEC 16 2010 This summary of 510(k) safety and effectiveness ination is being submitted in accordance with the requirements of SMDA 1990 and 21 CFR 807 - accessdata fda to 510(k) Summary for - accessdata fda

510(k) SUMMARY DEC 16 2010 This summary of 510(k) safety and effectiveness ination is being submitted in accordance with the requirements of SMDA 1990 and 21 CFR 807 - accessdata fda
510(k) SUMMARY DEC 3 0 2010 September 138t, 2010 Office of Device Evaluation U - accessdata fda
510(k) Summary ELitech Clinical Systems AMYLASE SL 1.Date ...
510(k) Summary for - accessdata fda