Air Compression Leg Massager (LF-FT001, LF-FT002-1, LF-FT003, LF-FT003-1, LF-FT004-1, LF-FT005-1, LF-FT006-1, LF-FT007, LF-FT008, LF-FT009, LF-FT010, LF-FT011, LF-FT012, LF-FT013, LF-FT014, LF-FT015, LF-FT016, UM-01, UM-02, UM-03, UM-03-1, UM-04-1, UM-05-1, UM-06-1, UM-07, UM-08, UM-09, UM-10, UM-11, UM-12, UM-13, UM-14, UM-15, UM-16, AI-01, AI-02, AI-03, AI-04, AI-05, AI-06, AI01, AI02, AI03, AI-07, AI-08, AI-09, AI-10, AI-11, AI-12, AI-13, AI-14)
K254200 is the FDA 510(k) clearance record for Air Compression Leg Massager (LF-FT001, LF-FT002-1, LF-FT003, LF-FT003-1, LF-FT004-1, LF-FT005-1, LF-FT006-1, LF-FT007, LF-FT008, LF-FT009, LF-FT010, LF-FT011, LF-FT012, LF-FT013, LF-FT014, LF-FT015, LF-FT016, UM-01, UM-02, UM-03, UM-03-1, UM-04-1, UM-05-1, UM-06-1, UM-07, UM-08, UM-09, UM-10, UM-11, UM-12, UM-13, UM-14, UM-15, UM-16, AI-01, AI-02, AI-03, AI-04, AI-05, AI-06, AI01, AI02, AI03, AI-07, AI-08, AI-09, AI-10, AI-11, AI-12, AI-13, AI-14), a class II device, cleared for Wenzhou Lingfeng Electronic Technology Co., Ltd. on under FDA product code IRP (Massager, Powered Inflatable Tube). FDA records list 2 510(k) clearances for Wenzhou Lingfeng Electronic Technology Co., Ltd., from to . As of , FDA records show no recalls naming K254200.
Clearance record
- Decision date
- Received
- (127 days to decision)
- Product code
- IRP Massager, Powered Inflatable Tube
- Regulation
- 21 CFR 890.5650
- Device class
- Class II
- Review panel
- Physical Medicine
- Applicant
- Wenzhou Lingfeng Electronic Technology Co., Ltd. #6 Puxi Industry Zone, Tongpu, Ruian, CN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code IRP
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 1 |
| December 2025 | 0 |
| January 2026 | 1 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 3 |
| May 2026 | 2 |
| June 2026 | 1 |
| July 2026 | 2 |
| August 2026 | 1 |
| September 2026 | 0 |
| October 2026 | 0 |
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