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510k Database
Manufacturers
US
Biosurge, Inc.
Medical Device Manufacturer
·
US , Rochester , NY
Biosurge, Inc. - FDA 510(k) Cleared Devices
5 submissions
·
5 cleared
·
Since 1987
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Biosurge, Inc.
General Hospital
✕
2
devices
1-2 of 2
Filters
Cleared
Nov 21, 1988
ASD SINGLE LUMEN NEEDLE
K884620
·
FMI
General Hospital
·
17d
Cleared
Feb 19, 1988
ASD-BIO ANTI-STICK DEVICE
K874602
·
FMI
General Hospital
·
102d
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Anesthesiology
2
General Hospital
2
Cardiovascular
1