Can-Am Surgical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Can-Am Surgical Corp. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Can-Am Surgical Corp. has 6 FDA 510(k) cleared medical devices. Based in Simi Valley, US.
Historical record: 6 cleared submissions from 1987 to 1987. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Can-Am Surgical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Can-Am Surgical Corp.
6 devices
Cleared
Apr 16, 1987
DISPOSABLE SYRINGE W/O NEEDLE
General Hospital
86d
Cleared
Apr 16, 1987
DISPOSABLE SYRINGE WITH NEEDLE
General Hospital
86d
Cleared
Apr 16, 1987
DISPOSABLE SYRINGE TUBERCULIN W/NEEDLE
General Hospital
86d
Cleared
Feb 27, 1987
A+MED DISPOSABLE NEEDLE
General Hospital
38d
Cleared
Feb 04, 1987
E-Z JECT INSULIN SYRINGE
General Hospital
33d
Cleared
Jan 21, 1987
AMG + MED LANCET
General & Plastic Surgery
19d