# Peca Labs

- Location (FDA's records): Pittsburgh, PA
- FDA decisions: 5 (2018–2024): 5 510(k) clearances
- Names in FDA's records: Peca Labs (4); Peca Labs, Inc. (1)
- Product codes: DSY (5)
- Predicates its devices cite: 5 (2 its own); citations of its devices by later devices: 2 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- W. L. Gore & Associates, Inc.: 1 (https://510kreport.com/company/w-l-gore-associates)
- Impra, Inc.: 1 (https://510kreport.com/company/impra)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)

## Its most-cited devices
- K202471: exGraft ePTFE Vascular Graft, exGraft Carbon ePTFE Vascular Graft (2020), cited by 1
- K221628: exGraft, exGraft Carbon (2022), cited by 1

## Recent decisions
- K233783: exGraft ePTFE Vascular Grafts, exGraft Carbon ePTFE Vascular Grafts (Jan 17, 2024)
- K221628: exGraft, exGraft Carbon (Aug 4, 2022)
- K202471: exGraft ePTFE Vascular Graft, exGraft Carbon ePTFE Vascular Graft (Dec 11, 2020)
- K183613: exGraft, exGraft Carbon (Apr 22, 2019)
- K180957: exGraft, exGraft Carbon ePTFE Vascular Grafts (Aug 21, 2018)

Source page: https://510kreport.com/company/peca-labs