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
- IKOHammer, Reflex, Powered2Product Code
- IKPChronaximeter2Product Code
- ISBStimulator, Muscle, Diagnostic2Product Code
- JFCSystem, Pressure Measurement, Intermittent1Product Code
- K924705FORCE SENSING ARRAY1Cleared 510(K)
- K925258DYNAMIC PRESSURE MONITOR 2000M AND 2000C1Cleared 510(K)
- K925052QA PRESSURE MEASUREMENT SYSTEM1Cleared 510(K)
- K915278CDG GAIT ANALYSES SYSTEM1Cleared 510(K)
- K914776OXFORD PRESSURE MONITOR/TALLEY PRESSURE MONITOR1Cleared 510(K)
- K913510MECHANICAL SHAPE SENSOR1Cleared 510(K)
- K881284COMPUTERIZED ORTHOPAEDIC PEDOTOPOGRAPHY MACHINE1Cleared 510(K)
- K8821392P-QDA FOOT PRESSURE SYSTEMS REAL TIME1Cleared 510(K)
- K861260PEDABAROGRAPH1Cleared 510(K)
- K831800TEXAS INTERFACE PRESSURE EVALUATOR-TIPE1Cleared 510(K)
Show All 11 Submissions
- 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
FORCE SENSING ARRAY
- Page Type
- Cleared 510(K)
- PDF* The FDA doesn't provide PDFs for all submissions.
- Analyzed PDF
- 510(k) Number
- K924705
- 510(k) Type
- Traditional
- Applicant
- FORCE SENSING SYSTEMS
- Country
- Canada
- FDA Decision
- Substantially Equivalent
- Decision Date
- 5/12/1993
- Days to Decision
- 237 days
- Submission Type
- Statement