510(k) K250817
- Device
- Coretech Compression System (Coretech RHB3003)
- Applicant
- Vive Health, LLC
- 510(k) number
- K250817
- Product code
- JOW
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2025-08-08
- Date received
- 2025-03-18
- Regulation
- 870.5800
- Classification name
- Sleeve, Limb, Compressible
- Medical specialty
- Cardiovascular
- Review panel
- Cardiovascular
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- Y
- Source
- FDA openFDA 510(k) dataset plus migrated FDA.report data
Related Records
Applicant Contact
- Contact
- Joe Fleming
- Address
- 8955 Fontana Del Sol Way Naples FL US 34109 34109
FDA Registration Numbers
- 3010190204
- 8043439
- 3012651177
- 3034205725
- 1061124
- 3010256111
- 3009350690
- 3004727093
- 3004183730
- 3007518069
- 3007420694
- 3012292104
- 3040278145
- 3012446970
- 1450371
- 3010246951
- 3009247326
- 1018470
- 3020163307
- 3014344059
- 1000589001
- 3011024991
- 3027977504
- 3008902816
- 3011118518
- 3009437400
- 8022590
- 3017264244
- 3005012805
- 3033511104
- 3013557562
- 3029923680
- 1423537
- 3005157379
- 2424387
- 3023215120
- 3018269548
- 3014947294
- 3016000973
- 9611425
- 3012174974
- 3012341425
- 3014491159
- 3015536408
- 3009176340
- 3021767551
- 1648700
- 3011529836
- 3013528589
- 3009155917
- 3017618673
- 2028253
- 3005619970
- 1649518
- 3032062344
- 3030153385
- 3038295706
- 3008773774
- 1063312
- 3011191255
- 3014579161
- 3034520
- 1417592
- 1928237
- 1061927
- 3031916218
- 3003619590
- 3010308146
- 3007699082
- 3004105270
- 3014834638
- 3011767724
- 3024685280
- 3012494290
- 1921846
- 3011539161
- 3011219270
- 3033981998
- 3029871637
- 8043817
Source Documents
FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON
Other 510(k) Records For Product Code JOW
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K250242 | Compression Therapy Device (LGT-2202DVT) | Guangzhou Longest Medical Technology Co., Ltd. | 2026-04-24 |
| K254267 | NanoPress 760A-BT (760A-BT) | Mego Afek , Ltd. | 2026-02-24 |
| K250974 | Bio Arterial Deluxe (IC-BAP-DX) | Bio Compression Systems, Inc. | 2025-12-12 |
| K250190 | Sequential Compression System (SCD600) | Shenzhen Comen Medical Instruments Co.,Ltd | 2025-12-08 |
| K251466 | 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 | Wellell, Inc. | 2025-10-28 |
| K251446 | PlasmaFlow X Compression Sleeve Device (XPF0001) | Manamed, LLC | 2025-09-17 |
| K251086 | PnueAira (PNCU-01) | Biotab, LLC | 2025-08-18 |
| K241096 | Venera 608 Deep Vein Thrombosis (DVT) Prevention System | Suzhou Minhua Medical Apparatus Supplies Co., Ltd. | 2025-01-15 |
| K240499 | ARTAIRA Arterial Compression Device (AACD01) | Airos Medical, Inc. | 2024-10-11 |
| K241746 | UMED REPROCESSED AIRCAST VENAFLOW FOOT CUFF; UMED REPROCESSED KENDALL SCD EXPRESS SLEEVE; UMED REPROCESSED AIRCAST ELITE CALF CUFF 3040 3050; UMED REPROCESSED CTC VP 501 CALF CUFF; UMED REPROCESSED CTC VP 520 FOOT CUFF | United Medical Resources, LLC | 2024-10-04 |
| K232640 | Venowave VW5 | Thermabright | 2024-06-25 |
| K234155 | Nimbl (model PD08-N1) | Tactile Medical | 2024-06-21 |
| K240125 | Therm-X (Home); Therm-X (AT) | Zenith Technical Innovations | 2024-06-21 |
| K232270 | DVT Motion Pneumatic Compression Device | Koge Micro Tech Co., Ltd. | 2024-03-06 |
| K240011 | Lymphedema Compression | Jkh Health Co., Ltd. | 2024-02-23 |