Multi-parameter detector
FDA 510(k) clearance K231116 · decided 2024-06-15
Clearance details
- K-number
- K231116
- Device name
- Multi-parameter detector
- Applicant
- Zhongshan Jinli Electronic Weighing Equipment Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2023-04-20
- Decision date
- 2024-06-15
- Days to decision
- 422 days
- Clearance type
- Traditional
- Product code
- MNW
- Device class
- 2
- Regulation number
- 870.2770
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Zhongshan, CN
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.