# K091933: Electro-Acupuncture: Aculife/Model Idoc-01

- Pathway: 510(k) (Special)
- Applicant: Inno-Health Technology, Inc.
- Decided: Apr 2, 2010 after 276 days
- Product code: BWK (Stimulator, Electro-Acupuncture)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K954334 (1996). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051197: Aculife, Model SMW-01, Inno-Health Technology, Inc. (2006) Summary page 1.

## Indications for use
The intended use of ACULIFE/Model IDOC-01 is an ELECTRO-ACUPUNCTURE DEVICE for use in the practice of acupuncture by qualified practitioners of acupuncture as determined by the states. ACULIFE/model IDOC-01 is intended for the stimulation at hands of patient.

Source page: https://510kreport.com/device/K091933
Methodology: https://510kreport.com/methodology