Single Use Cytology Brush
FDA 510(k) clearance K220063 · decided 2022-07-28
Clearance details
- K-number
- K220063
- Device name
- Single Use Cytology Brush
- Applicant
- Zhejiang Chuangxiang Medical Technology Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2022-01-10
- Decision date
- 2022-07-28
- Days to decision
- 199 days
- Clearance type
- Traditional
- Product code
- FDX
- Device class
- 2
- Regulation number
- 876.1500
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Hangzhou, CN
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.