Vesocclude Polymer Ligating Clip
FDA 510(k) clearance K152082 · decided 2016-02-26
Clearance details
- K-number
- K152082
- Device name
- Vesocclude Polymer Ligating Clip
- Applicant
- Vesocclude Medical, LLC
- Decision
- Substantially Equivalent
- Date received
- 2015-07-27
- Decision date
- 2016-02-26
- Days to decision
- 214 days
- Clearance type
- Traditional
- Product code
- FZP
- Device class
- 2
- Regulation number
- 878.4300
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Raleigh, NC, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.