# K970279: Race Car Tympanometer with Audiometer (AE-Rcaud I/Quik Tymp 1(AE-Quik 1)/Quick Tymp 2(AE-Quik 2)

- Pathway: 510(k) (Traditional)
- Applicant: American Electromedics Corp.
- Decided: Mar 18, 1997 after 54 days
- Product code: EWO (Audiometer)
- Device class: 2
- Regulation: 21 CFR 874.1050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 3 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K983051: American Electromedics Race CA Tympanometer/Audiometer with Integral Printer (1998), 0 descendants of its own
- K983049: American Electromedics Quik Tymp 1 (QT1) Tympanometer with Intergral Printer (1998), 0 descendants of its own
- K983048: American Electromedics Quik Tymp 2 (QT2) Tympanometer/Audiometer with Integral Printer (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K970279
Methodology: https://510kreport.com/methodology