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FDA Browser
by
Innolitics
Anesthesiology
Review Panel
Cardiovascular
Review Panel
Chemistry
Review Panel
Dental
Review Panel
Ear, Nose, Throat
Review Panel
Diagnostic Devices
CFR Sub-Part
ETK
Tube, Toynbee Diagnostic
1
Product Code
K
82
3774
WILSON EUSTACHIAN TUBAL, SONOGRAPH
1
Cleared 510(K)
Gastroenterology and Urology
Review Panel
General Hospital
Review Panel
Hematology
Review Panel
Immunology
Review Panel
Microbiology
Review Panel
Neurology
Review Panel
Obstetrical and Gynecological
Review Panel
Ophthalmic
Review Panel
Orthopedic
Review Panel
Pathology
Review Panel
Physical Medicine
Review Panel
Radiology
Review Panel
General and Plastic Surgery
Review Panel
Toxicology
Review Panel
Medical Genetics
Review Panel
Unknown
Review Panel
Last synced on 26 May 2023 at 11:04 pm
EN
/
diagnostic-devices
/
ETK
/
K823774
View Source
WILSON EUSTACHIAN TUBAL, SONOGRAPH
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K823774
510(k) Type
Traditional
Applicant
ANTARES TECHNICAL ASSOCIATES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1983
Days to Decision
34 days
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Chemistry
Dental
Ear, Nose, Throat
Diagnostic Devices
ETK
Tube, Toynbee Diagnostic
K
82
3774
WILSON EUSTACHIAN TUBAL, SONOGRAPH
Gastroenterology and Urology
General Hospital
Hematology
Immunology
Microbiology
Neurology
Obstetrical and Gynecological
Ophthalmic
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
EN
/
diagnostic-devices
/
ETK
/
K823774
View Source
WILSON EUSTACHIAN TUBAL, SONOGRAPH
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K823774
510(k) Type
Traditional
Applicant
ANTARES TECHNICAL ASSOCIATES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1983
Days to Decision
34 days