Epidural Anesthesia Needles, Spinal Anesthesia Needles, Combined Anesthesia Needles
FDA 510(k) clearance K171518 · decided 2018-01-05
Clearance details
- K-number
- K171518
- Device name
- Epidural Anesthesia Needles, Spinal Anesthesia Needles, Combined Anesthesia Needles
- Applicant
- Zhejiang Kindly Medical Devices Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2017-05-24
- Decision date
- 2018-01-05
- Days to decision
- 226 days
- Clearance type
- Traditional
- Product code
- BSP
- Device class
- 2
- Regulation number
- 868.5150
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- 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.