VesoFlow Lite DVT Compression Device— 510(k) K181217
Substantially EquivalentCaremed Supply, Inc.
FDA 510(k) clearance K181217 for VesoFlow Lite DVT Compression Device, Substantially Equivalent on 2018-08-05. Applicant: Caremed Supply, Inc..
Clearance details
- Applicant
- Caremed Supply, Inc.
- Product code
- Code JOW
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New Taipei City, TW
Data sourced from openFDA. This site is unofficial and independent of the FDA.