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
- K070926ELECTRODE/EXTENSION CABLES, MODELS ATAR2Cleared 510(K)
- K992372THE LEADAWAY2Cleared 510(K)
- K935260PHYSIOMETRIX CABLE ADAPTER MODIFICATION2Cleared 510(K)
- K873361LIFE-SPAN CABLE2Cleared 510(K)
- K834583CLEAR LEADS-RADIOTRANSPARENT WIRES2Cleared 510(K)
- K800934R2 ESU CABLE-ADAPTER MODELS 160,1612Cleared 510(K)
- 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
- 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
CLEAR LEADS-RADIOTRANSPARENT WIRES
- Page Type
- Cleared 510(K)
- 510(k) Number
- K834583
- 510(k) Type
- Traditional
- Applicant
- QUINTON, INC.
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 1/30/1984
- Days to Decision
- 32 days