Intelligence LaserComb
FDA 510(k) clearance K213789 · decided 2022-06-24
Clearance details
- K-number
- K213789
- Device name
- Intelligence LaserComb
- Applicant
- Yibin Yingtong Intelligent Technology Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2021-12-06
- Decision date
- 2022-06-24
- Days to decision
- 200 days
- Clearance type
- Traditional
- Product code
- OAP
- Device class
- 2
- Regulation number
- 890.5500
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- Yibin, CN
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.