The following data is part of a premarket notification filed by American Electromedics Corp. with the FDA for Ae-105d Diagnostic Tympanometer.
| Device ID | K894260 |
| 510k Number | K894260 |
| Device Name: | AE-105D DIAGNOSTIC TYMPANOMETER |
| Classification | Tester, Auditory Impedance |
| Applicant | AMERICAN ELECTROMEDICS CORP. 13 SAGAMORE PARK RD. Hudson, NH 03051 |
| Contact | Gleason |
| Correspondent | Gleason AMERICAN ELECTROMEDICS CORP. 13 SAGAMORE PARK RD. Hudson, NH 03051 |
| Product Code | ETY |
| CFR Regulation Number | 874.1090 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-06-20 |
| Decision Date | 1990-01-23 |