Bifurcated Needle— 510(k) K222385
Substantially EquivalentAnhui Tiankang Medical Technology Co., Ltd.
FDA 510(k) clearance K222385 for Bifurcated Needle, Substantially Equivalent on 2022-12-06. Applicant: Anhui Tiankang Medical Technology Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Anhui Tiankang Medical Technology Co., Ltd.
- Product code
- Code SCL
- Device class
- Class 2
- Regulation
- 21 CFR 880.5570
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tianchang, CN
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