PlasmaFlow
FDA 510(k) K160318 · Manamed, Inc.
510(k) numberK160318
Submission
- Device name
- PlasmaFlow
- Applicant
- Manamed, Inc.
Costa Mesa, CA, US - Received
- February 5, 2016
- Decision date
- April 1, 2016
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
- Third-party review
- Yes
Device classification
- Product code
- JOW – Sleeve, Limb, Compressible
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.5800
- Specialty
- Cardiovascular
Other 510(k)s with product code JOW
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261807 | Sequential Circulator (SC-4004-DL, SC-4008-DL)JOW · Traditional | Bio Compression Systems, Inc. | 09/11/2026SE |
| K254217 | AerloomJOW · Traditional | Evolym, LLC | 08/31/2026SE |
| K253555 | Flexitouch® Plus Advanced Pneumatic Compression SystemJOW · Traditional | Tactile Medical | 07/31/2026SE |
| K253386 | DVT GarmentJOW · Traditional | Vistar Medical Supplies Co., Ltd. | 06/25/2026SE |
| K250242 | Compression Therapy Device (LGT-2202DVT)JOW · Traditional | Guangzhou Longest Medical Technology Co., Ltd. | 04/24/2026SE |
| K254267 | NanoPress 760A-BT (760A-BT)JOW · Traditional | Mego Afek , Ltd. | 02/24/2026SE |
| K250974 | Bio Arterial Deluxe (IC-BAP-DX)JOW · Traditional | Bio Compression Systems, Inc. | 12/12/2025SE |
| K250190 | Sequential Compression System (SCD600)JOW · Traditional | Shenzhen Comen Medical Instruments Co.,Ltd | 12/08/2025SE |
| K251466 | VenAir, Sequential Compression System (9P-089000); VenAir, Sequential Compression System…JOW · Special | Wellell, Inc. | 10/28/2025SE |
| K251446 | PlasmaFlow X Compression Sleeve Device (XPF0001)JOW · Special | Manamed, LLC | 09/17/2025SE |
More from Manamed, LLC
| 510(k) | Device | Decision |
|---|---|---|
| K260944 | ManaCold Compression SystemIRP · Traditional | 08/12/2026SE |
| K251446 | PlasmaFlow X Compression Sleeve Device (XPF0001)JOW · Special | 09/17/2025SE |
| K231569 | ManaFlexx 2 (model: MF002-RX, MF002-OTC)NUH · Traditional | 11/03/2023SE |
| K222098 | ManaSport+IMI · Traditional | 03/08/2023SE |
| K210284 | ManaSportIMI · Traditional | 04/26/2022SE |
| K211253 | PlasmaWaveJOW · Special | 05/26/2021SE |
| K200353 | ManaFlowJOW · Traditional | 08/06/2020SE |
| K200351 | PlasmaFlightIRP · Traditional | 08/05/2020SE |
Questions and answers
When was PlasmaFlow cleared by the FDA?
PlasmaFlow (K160318) received a 510(k) decision of Substantially Equivalent on April 1, 2016, 56 days after the submission was received.
What is the product code of K160318?
The FDA product code is JOW – Sleeve, Limb, Compressible, a Class II (moderate risk) device regulated under 21 CFR 870.5800.