Jeesung Safety Syringe and Single Use Needles
FDA 510(k) clearance K152606 · decided 2016-06-28
Clearance details
- K-number
- K152606
- Device name
- Jeesung Safety Syringe and Single Use Needles
- Applicant
- Jeesung Medical Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2015-09-11
- Decision date
- 2016-06-28
- Days to decision
- 291 days
- Clearance type
- Traditional
- Product code
- MEG
- Device class
- 2
- Regulation number
- 880.5860
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Daejeon, KR
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.