Peca Labs is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Peca Labs - FDA 510(k) Cleared Devices
Recent clearances: exGraft, exGraft Carbon, exGraft ePTFE Vascular Graft, exGraft Carbon ePTFE Vascular Graft, exGraft, exGraft Carbon
4
Total
4
Cleared
0
Denied
Peca Labs has 4 FDA 510(k) cleared medical devices. Based in Pittsburgh, US.
Last cleared in 2022. Active since 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Peca Labs Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Peca Labs
4 devices
Cleared
Aug 04, 2022
exGraft, exGraft Carbon
Cardiovascular
59d
Cleared
Dec 11, 2020
exGraft ePTFE Vascular Graft, exGraft Carbon ePTFE Vascular Graft
Cardiovascular
105d
Cleared
Apr 22, 2019
exGraft, exGraft Carbon
Cardiovascular
117d
Cleared
Aug 21, 2018
exGraft, exGraft Carbon ePTFE Vascular Grafts
Cardiovascular
131d