exGraft ePTFE Vascular Grafts, exGraft Carbon ePTFE Vascular Grafts
Jan 2024
51d
Peca Labs, Inc.
1
Total
1
Cleared
0
Denied
Peca Labs, Inc. — FDA 510(k) Submissions
Peca Labs, Inc. has submitted 1 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Prosthesis, Vascular Graft, Of 6mm And Greater Diameter . Use the specialty filter in the sidebar to narrow results.
1 devices