Home › Device types › PFW
Stationary Ultrasonic Diathermy Device For Use In Applying Therapeutic Deep Heat
FDA product code PFW · Class 2 · Physical Medicine
42
Registered devices
2
Adverse events
0
Recalls
9
510(k) clearances
Devices with this code
sam 2.0 Long Duration Ultrasound Device for Home Use — ZETROZ SYSTEMS, LLCEcho GEL, TUBE, SINGLE, USND — THERMOTEK, INC.Echo Ultra Sound Gel Pod, Single — THERMOTEK, INC.Reusable Patch — NANOVIBRONIX INC.Echo Ultrasound Device (USA) — THERMOTEK, INC.sam 3.0 multi-hour continuous ultrasound device for home use — ZETROZ SYSTEMS, LLCechoRx, MANUAL, USER, SINGLE, USND — THERMOTEK, INC.Echo APPLICATOR, SINGLE, USND — THERMOTEK, INC.ManaMed Transducer Fixation Strap — Manamed, Inc.Echo Ultrasound Device (USA) — THERMOTEK, INC.PainShield MD Supplies Kit — NANOVIBRONIX INC.PainShield Plus 3.0 Driver — NANOVIBRONIX INC.Echo BOX, DRESSING & GEL POD PACK, USND, USA — THERMOTEK, INC.ManaMed Transducer Holder Patch — Manamed, Inc.PainShield — NANOVIBRONIX INC.Echo Ultrasound Device (PRC) — THERMOTEK, INC.PainShield 3.0 Actuator — NANOVIBRONIX INC.Echo POWER SUPPLY, CORD, SINGLE, USND — THERMOTEK, INC.Echo CTN, DRESSINGS, USND, USA, QTY 4 BOXES — THERMOTEK, INC.PainShield MD Plus — NANOVIBRONIX INC.Echo Ultrasound Device (PRC) — THERMOTEK, INC.sam(R) Advanced Gel Capture Patch — ZETROZ SYSTEMS, LLCsam 2.0 OA multi-hour continuous ultrasound device for home use — ZETROZ SYSTEMS, LLCsam X1 — ZETROZ SYSTEMS, LLC
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.