Company ยท US
Amplaid USA, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1978 to 2003. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jul 21, 2003 | K031978 | AMPLAID A756 SCREENING ADMITTANCE METER Amplaid | ETY |
| Aug 20, 1986 | K861014 | AMPLAID MK15 (EVOKED POTENTIAL SYSTEM) Amplaid USA, Inc. | GWL |
| Nov 25, 1983 | K832510 | EVOKED POTENTIALS SYSTEM MK10 Amplaid USA, Inc. | GWJ |
| Apr 29, 1981 | K810482 | SOMATOSENSORY STIMULATOR Amplaid USA, Inc. | GWF |
| Apr 29, 1981 | K810473 | MK6 ERA SYSTEM Amplaid USA, Inc. | GWJ |
| Mar 11, 1981 | K810481 | VISUAL PATTERN REVERSAL GEN. & PHOTIC S. Amplaid USA, Inc. | GWE |
| Dec 19, 1980 | K802963 | 101, 151, 161 PORTABLE AUDIOMETERS Amplaid USA, Inc. | EWO |
| Oct 10, 1980 | K802097 | SELF-RECORDING ADMITTANCE METER 709 Amplaid USA, Inc. | ETY |
| Nov 3, 1978 | K781667 | AMPLAID MARK 4 AND MARK 5 Amplaid USA, Inc. | GWJ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||