SPHYGMOMANOMETER
FDA 510(k) clearance K141392 · decided 2014-07-02
Clearance details
- K-number
- K141392
- Device name
- SPHYGMOMANOMETER
- Applicant
- Suzhou JJ Meter Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2014-05-27
- Decision date
- 2014-07-02
- Days to decision
- 36 days
- Clearance type
- Traditional
- Product code
- DXQ
- Device class
- 2
- Regulation number
- 870.1120
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Shenzhen, Guangdong, CN
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.