JIAJIAN ACUPUNCTURE NEEDLE
FDA 510(k) clearance K090199 · decided 2009-08-11
Clearance details
- K-number
- K090199
- Device name
- JIAJIAN ACUPUNCTURE NEEDLE
- Applicant
- Wuxi Jiajian Medical Instrument Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2009-01-27
- Decision date
- 2009-08-11
- Days to decision
- 196 days
- Clearance type
- Traditional
- Product code
- MQX
- Device class
- 2
- Regulation number
- 880.5580
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Wuxi, CN
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.