Anesthesiology
Review Panel
- CardiovascularReview Panel
- ChemistryReview Panel
- DentalReview Panel
- Ear, Nose, ThroatReview Panel
- MiscellaneousMiscellaneous
- ESIPolymer, Natural-Absorbable Gelatin Material3Product Code
- EWDProtector, Hearing (Insert)UProduct Code
- EWEProtector, Hearing (Circumaural)UProduct Code
- LEZAids, Speech Training For The Hearing Impaired (Ac-Powered And Patient-Contact)UProduct Code
- LFAAids, Speech Training For The Hearing Impaired (Battery-Operated Or Non-Patient)UProduct Code
- LFBButton, Nasal SeptalUProduct Code
- LRAHearing Aid, TactileUProduct Code
- LXVApparatus, Vestibular AnalysisUProduct Code
- K220231GyroStimUCleared 510(K)
- K200529OrionUCleared 510(K)
- K192652TRVUCleared 510(K)
- K183661ClearEdge Balance SystemUCleared 510(K)
- K190735EQ BalanceUCleared 510(K)
- K173669K-D BalanceUCleared 510(K)
- K121590VESTIBULAR ANALYSIS APPARATUSUCleared 510(K)
- K102364NYDIAG 200UCleared 510(K)
- K082634VERTIGONE BPPV GOGGLEUCleared 510(K)
- K081602DIZZYFIXUCleared 510(K)
- K071973EPLEY OMNIAXUCleared 510(K)
- K070676KOREBALANCE (KINESTHETIC ABILITY TRAINER)UCleared 510(K)
- K070085BALANCE REHABILITATION UNIT (BRU)UCleared 510(K)
- K971549VMT SYSTEMUCleared 510(K)
- K922037SYSTEM 2000, ROTATIONAL VESTIBULAR CHAIRUCleared 510(K)
- K911795KINESTHETIC ABILITY TRAINER (K.A.T., MODEL 1000)UCleared 510(K)
- K891008VESTIBULAR OCULAR REFLEX TEST EQUIPMENT(VORTEQ)UCleared 510(K)
- K884926BALANCE SYSTEMUCleared 510(K)
- K872093RVT-50 ROTARY CHAIR FOR VESTIBULAR TESTINGUCleared 510(K)
- K851744EQUITESTUCleared 510(K)
- K781268CHAIR, VESTIBULAR, ROTARY, COMPUT.UCleared 510(K)
- K771618COMPUTERIZED POSTURE PLATFORMUCleared 510(K)
- MCMImplant, Cochlear3Product Code
- MHEImplant, Auditory Brainstem3Product Code
- MJVDevice, Inflation, Middle EarUProduct Code
- MPVImplant, Hearing, Active, Middle Ear, Partially Implanted3Product Code
- MRKSystem, Imaging, Fluorescence3Product Code
- QNUTranscutaneous Electrical Nerve Stimulator For The Relief Of Congestion2Product Code
- OAAAid, Visual, For NauseaNProduct Code
- QLVField Generator Positioning Device1Product Code
- EPGStimulator, Transdermal3Product Code
- OAFImplant, Hearing, Active, Middle Ear, Totally Implanted3Product Code
- OAQElectronic Media, HyperacusisNProduct Code
- OWODrug-Eluting Sinus Stent3Product Code
- PGQCochlear Implant With Combined Electrical Stimulation And Acoustic Amplification3Product Code
- QJATympanostomy Tube Delivery Product With Drug3Product Code
- QOOVentilator Tubing And AccessoriesNProduct Code
- QOPRespiratory Humidifier For Emergency UseNProduct Code
- QOSContinuous VentilatorNProduct Code
- QOTEmergency VentilatorNProduct Code
- QOVCritical Care VentilatorNProduct Code
- QOXMulti-Patient Circuit ConnectorNProduct Code
- QQGOropharyngeal Electrical Stimulator2Product Code
- QVNCombined Acoustic And Electrical External Stimulation Device For The Relief Of Tinnitus2Product Code
- QXGCooperative Powered Surgical Assist Device For Ent Surgery2Product Code
- QZCExternal Mechanical Stimulator For The Relief Of Congestion2Product Code
- Submissions with No Product CodeMiscellaneous
- Subpart B—Diagnostic DevicesCFR Sub-Part
- Subpart D—Prosthetic DevicesCFR Sub-Part
- Subpart E—Neurological Surgical DevicesCFR Sub-Part
- Subpart E—Surgical DevicesCFR Sub-Part
- Subpart F—General Hospital and Personal Use Therapeutic DevicesCFR Sub-Part
- Subpart F—Therapeutic DevicesCFR Sub-Part
- Subpart G—General Hospital and Personal Use Miscellaneous DevicesCFR Sub-Part
- Subpart G—Miscellaneous DevicesCFR Sub-Part
- 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
- RadiologyReview Panel
- General and Plastic SurgeryReview Panel
- ToxicologyReview Panel
- Medical GeneticsReview Panel
- UnknownReview Panel
BALANCE SYSTEM
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K884926
- 510(k) Type
- Traditional
- Applicant
- CHATTANOOGA GROUP, INC.
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 2/27/1989
- Days to Decision
- 91 days