VESOFLOW PLUS DVT COMPRESSION DEVICE
FDA 510(k) clearance K141064 · decided 2014-12-04
Clearance details
- K-number
- K141064
- Device name
- VESOFLOW PLUS DVT COMPRESSION DEVICE
- Applicant
- Caremed Supply, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2014-04-24
- Decision date
- 2014-12-04
- Days to decision
- 224 days
- Clearance type
- Traditional
- Product code
- JOW
- Device class
- 2
- Regulation number
- 870.5800
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- New Taipei City, TW
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.