# Medical Engineering and Development Institute

- Location (FDA's records): West Lafayette, IN
- FDA decisions: 6 (1989–1990): 6 510(k) clearances
- Product codes: GCC (2), DRE (1), DYB (1), GAD (1), LJT (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)
- Edwards Lifesciences, LLC: 1 (https://510kreport.com/company/edwards-lifesciences)
- Endologix, Inc.: 1 (https://510kreport.com/company/endologix)

## Its most-cited devices
- K902469: Byrd Dilator Sheath Set - Teflon (1990), cited by 3

## Recent decisions
- K902477: Workstation Femoral Intravascular Retrieval Set (Aug 24, 1990)
- K902469: Byrd Dilator Sheath Set - Teflon (Aug 23, 1990)
- K902502: Byrd Stainless Steel Dilator (Aug 7, 1990)
- K895030: Life-Line (TM) Vascular Access System (Apr 17, 1990)
- K893480: Byrd Extractor Set (Jun 23, 1989)
- K890820: Locking Wire Guide Stylet (Mar 22, 1989)

Source page: https://510kreport.com/company/medical-engineering-and-development-institute