# Weaver & Co.

- Location (FDA's records): Aurora, CO
- FDA decisions: 4 (1978–1989): 4 510(k) clearances
- Product codes: GYB (2), DRX (1), GXY (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
- Compumedics USA, Ltd.: 1 (https://510kreport.com/company/compumedics-usa)
- Electro-Cap Intl., Inc.: 1 (https://510kreport.com/company/electro-cap-intl)
- Wuhan Greentek Pty, Ltd.: 1 (https://510kreport.com/company/wuhan-greentek)

## Its most-cited devices
- K883149: TEN20 Conductive (1988), cited by 2
- K885306: Nuprep (1989), cited by 1

## Recent decisions
- K885306: Nuprep (Feb 23, 1989)
- K883149: TEN20 Conductive (Sep 28, 1988)
- K874075: PT-100-30 Somatosensory Stimulating Electrode (Oct 20, 1987)
- K781989: Omniprep (Dec 15, 1978)

Source page: https://510kreport.com/company/weaver