The following data is part of a premarket notification filed by American Electromedics Corp. with the FDA for American Electromedics Quik Tymp 1 (qt1) Tympanometer With Intergral Printer.
Device ID | K983049 |
510k Number | K983049 |
Device Name: | AMERICAN ELECTROMEDICS QUIK TYMP 1 (QT1) TYMPANOMETER WITH INTERGRAL PRINTER |
Classification | Tester, Auditory Impedance |
Applicant | AMERICAN ELECTROMEDICS CORP. P.O. BOX 9169 Chico, CA 95927 |
Contact | Frank Ferguson |
Correspondent | Frank Ferguson AMERICAN ELECTROMEDICS CORP. P.O. BOX 9169 Chico, CA 95927 |
Product Code | ETY |
CFR Regulation Number | 874.1090 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-09-01 |
Decision Date | 1998-11-18 |
Summary: | summary |