The following data is part of a premarket notification filed by American Electromedics Corp. with the FDA for Immittance Meter, Model Ae-105d/s.
Device ID | K905212 |
510k Number | K905212 |
Device Name: | IMMITTANCE METER, MODEL AE-105D/S |
Classification | Tester, Auditory Impedance |
Applicant | AMERICAN ELECTROMEDICS CORP. 13 SAGAMORE PARK RD. Hudson, NH 03051 |
Contact | Thomas M Gleason |
Correspondent | Thomas M 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 | 1990-11-20 |
Decision Date | 1991-02-19 |