The following data is part of a premarket notification filed by American Electromedics Corp. with the FDA for Automatic Impedance Meter Ae-205.
Device ID | K924934 |
510k Number | K924934 |
Device Name: | AUTOMATIC IMPEDANCE METER AE-205 |
Classification | Tester, Auditory Impedance |
Applicant | AMERICAN ELECTROMEDICS CORP. 13 COLUMBUS DR. SUITE 18 Amherst, NH 03031 |
Contact | Gleason |
Correspondent | Gleason AMERICAN ELECTROMEDICS CORP. 13 COLUMBUS DR. SUITE 18 Amherst, NH 03031 |
Product Code | ETY |
CFR Regulation Number | 874.1090 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-09-30 |
Decision Date | 1993-01-21 |