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510k Database
Manufacturers
US
Medway
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Medical Device Manufacturer
·
US , Franklin , TN
Medway - FDA 510(k) Cleared Devices
5 submissions
·
5 cleared
·
Since 1991
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medway
General Hospital
✕
4
devices
1-4 of 4
Filters
Cleared
Apr 29, 1994
HOME AMB-ALERT
K934344
·
KMI
General Hospital
·
233d
Cleared
Oct 28, 1991
FLEX-IV
K911251
·
FOZ
General Hospital
·
221d
Cleared
Sep 13, 1991
AMB-ALERT
K911079
·
KMI
General Hospital
·
186d
Cleared
Jun 06, 1991
COMFOR-BOARD
K910880
·
KMK
General Hospital
·
97d
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5
General Hospital
4
Anesthesiology
1