# Medac, Inc.

- Location (FDA's records): Tualatin, OR
- FDA decisions: 10 (1987–1988): 10 510(k) clearances
- Product codes: DRO (8), DRT (1), LDD (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
- K874319: Monitor, Electrographic (Mar 7, 1988)
- K874447: Disposable Gel Defibrillation/External Pacing Elec (Jan 27, 1988)
- K874090: 300M Ecg Monitro/Transcutaneous Pacemaker (Dec 15, 1987)
- K874091: 360D DC Defibrillator (Nov 23, 1987)
- K871176: Pace 10 Non-Invasive External Pacemaker (Apr 23, 1987)
- K864985: Dispos Gel External Pacing Electrode/Low Impedance (Mar 10, 1987)
- K864987: Dispos Gel External Pacing Electrode/HI Impedance (Mar 3, 1987)
- K864986: Etp 300 Non-Invasive External Pacemaker (Mar 3, 1987)

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