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FDA Browser
by
Innolitics
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CFR Sub-Part
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IKN
Electromyograph, Diagnostic
2
Product Code
IKT
Electrode, Needle, Diagnostic Electromyograph
2
Product Code
LYH
Arthrometer
1
Product Code
K
94
3197
KT1000/S KNEE LIGAMENT ARTHROMETER
1
Cleared 510(K)
K
94
2059
KT2000 KNEE LIGAMENT ARTHROMETER
1
Cleared 510(K)
K
88
1876
DYNAMIC CRUCIATE TESTER
1
Cleared 510(K)
K
83
4462
GENUCOM
1
Cleared 510(K)
K
81
2806
KT-1000 DEVICE
1
Cleared 510(K)
Physical Medicine Prosthetic Devices
CFR Sub-Part
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CFR Sub-Part
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Review Panel
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Unknown
Review Panel
Last synced on 2 June 2023 at 11:04 pm
NE
/
physical-medicine-diagnostic-devices
/
LYH
/
K881876
View Source
DYNAMIC CRUCIATE TESTER
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881876
510(k) Type
Traditional
Applicant
DYONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/1988
Days to Decision
197 days
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Chemistry
Dental
Ear, Nose, Throat
Gastroenterology and Urology
General Hospital
Hematology
Immunology
Microbiology
Neurology
Cardiovascular Diagnostic Devices
Cardiovascular Monitoring Devices
Cardiovascular Therapeutic Devices
Diagnostic Devices
Miscellaneous
Neurological Diagnostic Devices
Neurological Surgical Devices
Neurological Therapeutic Devices
Physical Medicine Diagnostic Devices
IKN
Electromyograph, Diagnostic
IKT
Electrode, Needle, Diagnostic Electromyograph
LYH
Arthrometer
K
94
3197
KT1000/S KNEE LIGAMENT ARTHROMETER
K
94
2059
KT2000 KNEE LIGAMENT ARTHROMETER
K
88
1876
DYNAMIC CRUCIATE TESTER
K
83
4462
GENUCOM
K
81
2806
KT-1000 DEVICE
Physical Medicine Prosthetic Devices
Physical Medicine Therapeutic Devices
Surgical Devices
Therapeutic Devices
Obstetrical and Gynecological
Ophthalmic
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
NE
/
physical-medicine-diagnostic-devices
/
LYH
/
K881876
View Source
DYNAMIC CRUCIATE TESTER
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881876
510(k) Type
Traditional
Applicant
DYONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/1988
Days to Decision
197 days