The following data is part of a premarket notification filed by American Electromedics Corp. with the FDA for The Automatic Impedance Meter,model Ae-208d/s.
Device ID | K930164 |
510k Number | K930164 |
Device Name: | THE AUTOMATIC IMPEDANCE METER,MODEL AE-208D/S |
Classification | Tester, Auditory Impedance |
Applicant | AMERICAN ELECTROMEDICS CORP. 13 COLUMBUS DR. SUITE 18 Amherst, NH 03031 |
Contact | Noel Wren |
Correspondent | Noel Wren 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 | 1993-01-13 |
Decision Date | 1993-04-23 |