Product code BWK— Unknown
ACULIFE, MODEL SMW-01
- Classification name
- Stimulator, Electro-Acupuncture
- Device class
- Unclassified
- Advisory panel
- Unknown
- Total cleared
- 23
- First cleared
- Most recent
Market context for product code BWK
FDA has cleared devices under product code BWK between 1979 and 2025, filed by 17 applicant companies. No FDA device recalls reference this product code.
Clearances per year
last 15 years- 2025
- 2022
- 2021
- 2017
- 2016
- 2015
- 2014
- 2013
- 2010
- 2009
- 2008
- 2006
- 2002
- 1984
- 1979
Top applicants under product code BWK
Recent clearances under product code BWK
- K244030 — Needle Stimulator (CMNS6-1 PLUS, CMNS6-3)
- K220153 — Needle Stimulator (Model: RJNS6-1)
- K202861 — Needle Stimulator
- K200636 — AXUS ES-5 Electro-Acupuncture Device
- K170391 — ANSiStim-PP
- K152571 — Stivax
- K141168 — ANSISTIM
- K133980 — PANTHEON ELECTROSTIMULATOR
- K140530 — Electro Auricular Device
- K140788 — P-STIM
- K130768 — JIAJIAN CMN STIMULATOR
- K122812 — JIAJIAN ELECTRO-ACUPUNCTURE STIMULATORS
- K093322 — MULTI-PURPOSE HEALTH DEVICE
- K091933 — ELECTRO-ACUPUNCTURE: ACULIFE/MODEL IDOC-01
- K091875 — E-PULSE
- K081943 — MODEL ES-130
- K050123 — P-STIM SYSTEM
- K051197 — ACULIFE, MODEL SMW-01
- K014273 — ACUSTIM
- K840983 — PULSELIFE STIMULATOR
- K840995 — ACUPUNCTURE INSOLES
- K832634 — SELECTRODE SYSTEM
- K781651 — HEALTH POINT
Data sourced from openFDA. This site is unofficial and independent of the FDA.