VenAir, Sequential Compression System (9P-089000); VenAir, Sequential Compression System (PM01D01 / Calf garment (S)); VenAir, Sequential Compression System (PM01E01 / Calf garment (M)); VenAir, Sequential Compression System (PM01F01 / Calf garment (L)); VenAir, Sequential Compression System (PM01G01 / Thigh garment (S)); VenAir, Sequential Compression System (PM01H01 / Thigh garment (M)); VenAir, Sequential Compression System (PM01I01 / Thigh garment (L)); VenAir, Sequential Compr
K251466 is the FDA 510(k) clearance record for VenAir, Sequential Compression System (9P-089000); VenAir, Sequential Compression System (PM01D01 / Calf garment (S)); VenAir, Sequential Compression System (PM01E01 / Calf garment (M)); VenAir, Sequential Compression System (PM01F01 / Calf garment (L)); VenAir, Sequential Compression System (PM01G01 / Thigh garment (S)); VenAir, Sequential Compression System (PM01H01 / Thigh garment (M)); VenAir, Sequential Compression System (PM01I01 / Thigh garment (L)); VenAir, Sequential Compr, a class II device, cleared for Wellell, Inc. on under FDA product code JOW (Sleeve, Limb, Compressible). FDA records list 2 510(k) clearances for Wellell, Inc., from to . As of , FDA records show no recalls naming K251466.
Clearance record
- Decision date
- Received
- (168 days to decision)
- Product code
- JOW Sleeve, Limb, Compressible
- Regulation
- 21 CFR 870.5800
- Device class
- Class II
- Review panel
- Cardiovascular
- Applicant
- Wellell, Inc. # 9, Min Sheng St., Tu-Cheng Dist., New Taipei City, TW
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code JOW
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 2 |
| January 2026 | 0 |
| February 2026 | 1 |
| March 2026 | 0 |
| April 2026 | 1 |
| May 2026 | 0 |
| June 2026 | 1 |
| July 2026 | 1 |
| August 2026 | 1 |
| September 2026 | 1 |
| October 2026 | 0 |
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