Empi
Empi holds FDA 510(k) medical device clearances, first cleared 1977, most recent 2010.
Top product codes for Empi
Recent clearances by Empi
- K093324 — EMPI CONTINUUM
- K090922 — EMPI ACTIVE TRANSCUTANEOUS NERVE STIMULATOR
- K072946 — HYBRESIS IONTOPHORESIS DRUG DELIVERY SYSTEM
- K070427 — DUPEL TRANSPORT IONTOPHORESIS SYSTEM
- K061650 — SELECT TENS, MODEL 4600S
- K041920 — INFINITY PLUS ELECTROTHERAPY SYSTEM
- K042057 — INFINITY ELECTROTHERAPY SYSTEM
- K030395 — EMPI ACTION PATCH IONTOPHORESIS SYSTEM
- K021100 — 300 PV COMPLETE ELECTROTHERAPY SYSTEM
- K991991 — DUPEL IONTOPHORESIS SYSTEM
- K983484 — DUPEL B.L.U.E. SMALL IONTOPHORESIS ELECTRODE
- K983206 — SMALL VAGINAL/RECTAL ELECTRODE
- K972054 — INNOVA RECTAL REUSABLE ELECTRODE/COMFORTPULSE REGULAR OR SMALL REUSABLE ELECTRODE
- K971527 — INNOSENSE PELVIC FLOOR STIMULATION AND ELECTROMYOGRAPHY SYSTEM
- K970491 — DUPEL II BUFFERED IONTOPHORESIS ELECTRODES
- K970307 — MINNOVA PELVIC FLOOR STIMULATION SYSTEM
- K970203 — EPIX VT
- K964577 — INNOVA COMFORTPULSE VAGINAL ELECTRODE (199204)/INNOVA COMFORTPULSE SMALL VAGINAL ELECTRODE(199205)
- K951951 — FOCUS MODEL 795 UNIT
- K954272 — INNOVA RECTAL STIMULATON ELECTRODE
- K951903 — EPIX XL TENS UNIT
- K952688 — INNOVA RECTAL OR SMALL VAGINAL EMG SENSING ELECTRODE
- K941911 — INNOVA PELVIC FLOOR STIMULATION SYSTEM
- K940091 — INNOVA VAGINAL EMG SENSING ELECTRODE
- K941389 — EMPI TAPE PATCHES
- K915444 — DUPEL IONTOPHORESIS DEVICE
- K912015 — TBD, EMPI BUFFERED IONTOPHORESIS ELECTRODED MDL. 3
- K912014 — TBD, EMPI BUFFERED IONTOPHORESIS ELECTRODES MDL. 2
- K910081 — TBD
- K903093 — IONTOPHORESIS DEVICE
- K902195 — TBD TENS REUSABLE ELECTRODE
- K901102 — MODIFIED ISLAND PIN TENS DISPOSABLE ELECTRODE
- K901103 — MODIFIED ISLAND SNAP TENS DISPOSABLE ELECTRODE
- K896703 — TBD IONTOPHORESIS ELECTRODE
- K896485 — MODIFIED ISLAND TENS DISP. ELECTRODE FOR SNAP CONN
- K890604 — EMPI, MODEL 489, TENS
- K890605 — EMPI ISLAND TENS ELECTRODE
- K890614 — EMPI MULTIDAY TENS DISPOSABLE ELECTRODE
- K890747 — EMPI REUSEABLE PIN-STYLE TENS ELECTRODE
- K882631 — EMPI MODEL 727,NMS
- K881114 — EMPI MODEL 989, TENS
- K870168 — EMPI LOGIX MODEL 712 NMS, TENS
- K864010 — EMPI MODEL 712, LOGIX(TM), NMS
- K862231 — EMPI, MODEL 1000 HAND HELD ELECTRODE
- K861830 — EMPI MODEL GLS 450, TENS
- K861451 — EMPI MODEL 720 NMS, TENS
- K854774 — EMPI MODEL 720 NMS
- K854775 — EMPI MODEL 730 NMS
- K854513 — EMPI, NMS/SUE CUTANEOUS ELECTRODE
- K851331 — EMPI MODEL 100, CPM(POWER EXCERISE EQUIPMENT)
- K841382 — EMPI MODEL 712, LOGIX, NMS
- K841045 — EMPI MODEL 984 BASIX, TENS
- K822224 — EMPI SINGLE USE
- K813501 — TRANSCUTANEOUS ELEC. NERVE STIMULATOR
- K811395 — EMPI MODEL 710, NMS
- K802507 — TENSMATE EMPIMODEL 9980
- K801112 — EMPI MODEL 910S, TENS
- K800380 — FES ORTHOSIS MODEL NO. 2000
- K792522 — MODEL 980D TENS NEUROPACER
- K771885 — IMPORTED PAIN CONTROL DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.