510(k) K213313
K213313 is an FDA 510(k) premarket notification submitted by Dalian Labtek Science & Development Co., Ltd. for the device "Veinoflow SCD (Model: LBTK-M-I 5006)". The FDA issued a decision of Substantially Equivalent on Feb 9, 2022. The device falls under product code JOW (Sleeve, Limb, Compressible), a Class II device regulated under 21 CFR 870.5800. Dalian Labtek Science & Development Co., Ltd. has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 9, 2022
- Date Received
- Oct 4, 2021
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Sleeve, Limb, Compressible
- Device Class
- Class II
- Regulation Number
- 870.5800
- Review Panel
- CV
- Submission Type
- 510(k)