# Tdk Corp.

- Location (FDA's records): 272 01, Japan, JP
- FDA decisions: 6 (1984–1988): 6 510(k) clearances
- Product codes: DRX (5), DRS (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K883643: TDK Ecg Electrode, Mel-10L (Nov 17, 1988)
- K882904: TDK Electrode Mel-20-1, Mel-20-3, Mel-20-5 (Oct 5, 1988)
- K870834: TDK Ecg Electrode Mel-10 (Mar 23, 1987)
- K863369: Mel-16-1, Mel-16-3 & Mel-16-5 TDK Ecg Electrodes (Jan 6, 1987)
- K854596: TDK Ecg Electrode Mel-08-09 & -11 (May 7, 1986)
- K833899: TDK Ecg Electrode Mel-08 (Feb 10, 1984)

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