Anesthesiology
Review Panel
- CardiovascularReview Panel
- ChemistryReview Panel
- DentalReview Panel
- Ear, Nose, ThroatReview Panel
- Gastroenterology and UrologyReview Panel
- General HospitalReview Panel
- HematologyReview Panel
- ImmunologyReview Panel
- MicrobiologyReview Panel
- NeurologyReview Panel
- Obstetrical and GynecologicalReview Panel
- OphthalmicReview Panel
- OrthopedicReview Panel
- PathologyReview Panel
- Physical MedicineReview Panel
- MiscellaneousMiscellaneous
- Subpart B—Physical Medicine Diagnostic DevicesCFR Sub-Part
- IKDCable, Electrode2Product Code
- IKETransducer, Miniature Pressure1Product Code
- IKKSystem, Isokinetic Testing And Evaluation2Product Code
- K123746AMES THERAPY DEVICE2Cleared 510(K)
- K952090HUMAC SYSTEM2Cleared 510(K)
- K951770BIODEX SYSTEM 3 MODEL S3S-AP AND MODEL S3D-3AP2Cleared 510(K)
- K951916CC RIDER, MODEL ME1802Cleared 510(K)
- K950095CYBEX 7702Cleared 510(K)
- K942229MOTIVATOR FTR 20002Cleared 510(K)
- K944732DEXTER ISOKINETIC2Cleared 510(K)
- K924414THE BTE DYNAMIC LIFT2Cleared 510(K)
- K923350CLOSED CHAIN ATTACHMENT, MODEL #820-5202Cleared 510(K)
- K922772TWO POSITION ROLL-UP BACK ATTACHMENT CHAIR2Cleared 510(K)
Show All 61 Submissions
- IKOHammer, Reflex, Powered2Product Code
- IKPChronaximeter2Product Code
- ISBStimulator, Muscle, Diagnostic2Product Code
- JFCSystem, Pressure Measurement, Intermittent1Product Code
- KHXPlatform, Force-Measuring1Product Code
- OALExercise Equipment, Powered, Emg-Triggered2Product Code
- Subpart D—Physical Medicine Prosthetic DevicesCFR Sub-Part
- Subpart E—Surgical DevicesCFR Sub-Part
- Subpart F—Neurological Therapeutic DevicesCFR Sub-Part
- Subpart F—Physical Medicine Therapeutic DevicesCFR Sub-Part
- RadiologyReview Panel
- General and Plastic SurgeryReview Panel
- ToxicologyReview Panel
- Medical GeneticsReview Panel
- UnknownReview Panel
MOTIVATOR FTR 2000
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K942229
- 510(k) Type
- Traditional
- Applicant
- HOGAN & HARTSON
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 2/27/1995
- Days to Decision
- 297 days
- Submission Type
- Summary