Amplaid USA, Inc.
Amplaid USA, Inc. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1986.
Top product codes for Amplaid USA, Inc.
Recent clearances by Amplaid USA, Inc.
- K861014 — AMPLAID MK15 (EVOKED POTENTIAL SYSTEM)
- K832510 — EVOKED POTENTIALS SYSTEM MK10
- K810473 — MK6 ERA SYSTEM
- K810482 — SOMATOSENSORY STIMULATOR
- K810481 — VISUAL PATTERN REVERSAL GEN. & PHOTIC S.
- K802963 — 101, 151, 161 PORTABLE AUDIOMETERS
- K802097 — SELF-RECORDING ADMITTANCE METER 709
- K781667 — AMPLAID MARK 4 AND MARK 5
Data sourced from openFDA. This site is unofficial and independent of the FDA.