SYVEK RADIAL BAND
FDA 510(k) clearance K132293 · decided 2014-07-31
Clearance details
- K-number
- K132293
- Device name
- SYVEK RADIAL BAND
- Applicant
- Marine Polymer Technologies
- Decision
- Substantially Equivalent
- Date received
- 2013-07-23
- Decision date
- 2014-07-31
- Days to decision
- 373 days
- Clearance type
- Traditional
- Product code
- DXC
- Device class
- 2
- Regulation number
- 870.4450
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Danvers, MA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.