KINGLI ACUPUNCTURE NEEDLE— 510(k) K990406
Substantially EquivalentUnited Pacific Co., Ltd.
FDA 510(k) clearance K990406 for KINGLI ACUPUNCTURE NEEDLE, Substantially Equivalent on 1999-04-16. Applicant: United Pacific Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- United Pacific 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
- Alhambra, CA, US
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