ANEROID SPHYGMOMANOMETER
FDA 510(k) clearance K173246 · decided 2018-05-30
Clearance details
- K-number
- K173246
- Device name
- ANEROID SPHYGMOMANOMETER
- Applicant
- Wenzhou Bokang Instruments Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2017-10-06
- Decision date
- 2018-05-30
- Days to decision
- 236 days
- Clearance type
- Abbreviated
- Product code
- DXQ
- Device class
- 2
- Regulation number
- 870.1120
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Wenzhou, CN
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.