Medical Device Manufacturer · US , Fort Myers , FL

P/L Biomedical - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1997
3
Total
3
Cleared
0
Denied

P/L Biomedical has 3 FDA 510(k) cleared medical devices. Based in Fort Myers, US.

Historical record: 3 cleared submissions from 1997 to 2012. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by P/L Biomedical Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - P/L Biomedical

3 devices
1-3 of 3
Cleared Oct 25, 2012
CLICKFINE PEN NEEDLE
K122969 · FMI
General Hospital · 29d
Cleared Oct 25, 2012
CLICKFINE PEN NEEDLE
K122971 · FMI
General Hospital · 29d
Cleared Aug 26, 1997
MAERSK MEDICAL PURELINE COMFORT SUBCUTANEOUS INFUSION SET
K972135 · FPA
General Hospital · 81d
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