# K983049: American Electromedics Quik Tymp 1 (QT1) Tympanometer with Intergral Printer

- Pathway: 510(k) (Traditional)
- Applicant: American Electromedics Corp.
- Decided: Nov 18, 1998 after 78 days
- Product code: ETY (Tester, Auditory Impedance)
- Device class: 2
- Regulation: 21 CFR 874.1090
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K970279 (1997). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K970279: Race Car Tympanometer with Audiometer (AE-Rcaud I/Quik Tymp 1(AE-Quik 1)/Quick Tymp 2(AE-Quik 2), American Electromedics Corp. (1997) Summary page 1.

## Indications for use
The American Electromedics Quik Tymp 1 (QT1) Tympanometer With Integral Printer is intended to be used in conducting hearing evaluations and assisting in the diagnosis of possible otologic disorders.

Source page: https://510kreport.com/device/K983049
Methodology: https://510kreport.com/methodology