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.. Device class: 2.
Clearance details
- Applicant
- Caremed Supply, Inc.
- Product code
- Code JOW
- Device class
- Class 2
- Regulation
- 21 CFR 870.5800
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New Taipei City, TW
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