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- 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
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TWO POSITION ROLL-UP BACK ATTACHMENT CHAIR
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K922772
- 510(k) Type
- Traditional
- Applicant
- BIODAN MEDICAL SYSTEMS, LTD.
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 7/13/1992
- Days to Decision
- 34 days
- Submission Type
- Statement