TIANXIE— 510(k) K003748
Substantially EquivalentSuzhou Tianyi Acupuncture Instruments Co., Ltd.
FDA 510(k) clearance K003748 for TIANXIE, Substantially Equivalent on 2001-01-26. Applicant: Suzhou Tianyi Acupuncture Instruments Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Suzhou Tianyi Acupuncture Instruments Co., Ltd.
- Product code
- Code MQX
- Device class
- Class 2
- Regulation
- 21 CFR 880.5580
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Costa Mesa, CA, US
Recent devices under product code MQX
view all- K162566 — AIK Sterile Acupuncture Needles for Single Use
- K142760 — Acuzone Acupuncture Needles, KSC DB Plus Acupuncture Needles
- K150903 — EACU, ZAGU, JOCU, EAKU, BALANCE, TEMPO, ACUZONE, SMART, PRIME, ACUSTAR, ACUKING, Myotech Dry, Red Coral Premium, Red Coral J-Type, Red Coral Natural
- K142920 — KM Needles (Acupuncture Needle)
- K141473 — SMC ACUPUNCTURE NEEDLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.