# Amplaid USA, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 8 (1978–1986): 8 510(k) clearances
- Product codes: GWJ (3), EWO (1), ETY (1), GWL (1), GWE (1), GWF (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
- Amplifon S.P.A.: 3 (https://510kreport.com/company/amplifon)

## Its most-cited devices
- K861014: Amplaid MK15 (Evoked Potential System) (1986), cited by 2
- K802097: Self-Recording Admittance Meter 709 (1980), cited by 1

## Recent decisions
- K861014: Amplaid MK15 (Evoked Potential System) (Aug 20, 1986)
- K832510: Evoked Potentials System MK10 (Nov 25, 1983)
- K810473: MK6 Era System (Apr 29, 1981)
- K810482: Somatosensory Stimulator (Apr 29, 1981)
- K810481: Visual Pattern Reversal Gen. & Photic S. (Mar 11, 1981)
- K802963: 101, 151, 161 Portable Audiometers (Dec 19, 1980)
- K802097: Self-Recording Admittance Meter 709 (Oct 10, 1980)
- K781667: Amplaid Mark 4 and Mark 5 (Nov 3, 1978)

Source page: https://510kreport.com/company/amplaid-usa