Encircle Compression Therapy Stocking
K122485 is the FDA 510(k) clearance record for ENCIRCLE COMPRESSION THERAPY STOCKING, a class II device, cleared for Encircle Medical Devices , Ltd. on under FDA product code DWL (Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)). FDA records list one 510(k) clearance for Encircle Medical Devices , Ltd. As of , FDA records show no recalls naming K122485.
Clearance record
- Decision date
- Received
- (252 days to decision)
- Product code
- DWL Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)
- Regulation
- 21 CFR 880.5780
- Device class
- Class II
- Review panel
- General Hospital
- Applicant
- Encircle Medical Devices , Ltd. 2400 Via Carillo, Palos Verdes Estates CA
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code DWL
Trailing 12 monthsFDA records hold no clearances under product code DWL in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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