ASAHI STERILE ACUPUNCTURE NEEDLE TYPE S— 510(k) K000740
Substantially EquivalentAsahi Iryoki Co., Ltd.
FDA 510(k) clearance K000740 for ASAHI STERILE ACUPUNCTURE NEEDLE TYPE S, Substantially Equivalent on 2000-04-12. Applicant: Asahi Iryoki Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Asahi Iryoki 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
- White Plains, NY, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.