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by
Innolitics
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2
Product Code
HRW
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1
Product Code
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1
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16
2412
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07
3154
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K
05
2309
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04
2889
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01
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2
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98
1730
DIGIT-GRIP WITH LCD, MODEL NUMBER DGR 002
2
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98
0363
ORO-FACIAL MYOGRAPHIC MEASUREMENT INSTRUMENT (OMMI)
2
Cleared 510(K)
K
96
4933
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2
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K
96
4685
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2
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K
93
5757
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2
Cleared 510(K)
Show All 36 Submissions
NKI
Goniometer With Electrodes
2
Product Code
Miscellaneous
Miscellaneous
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Last synced on 26 May 2023 at 11:04 pm
NE
/
diagnostic-devices
/
LBB
/
K981730
View Source
DIGIT-GRIP WITH LCD, MODEL NUMBER DGR 002
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981730
510(k) Type
Traditional
Applicant
NK BIOTECHNICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/1998
Days to Decision
63 days
Submission Type
Statement
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
PDQ
Neurosurgical Nerve Locator
HRW
Dynamometer, Nonpowered
KQW
Goniometer, Nonpowered
KQX
Goniometer, Ac-Powered
LBB
Dynamometer, Ac-Powered
K
16
2412
Hoggan Scientific® microFET2™
K
07
3154
FACTS HAND AND PINCH GRIP COMBO
K
05
2309
DIGITAL HAND DYNAMOMETER, MODEL SH5003; DIGITAL PINCH GAUGE, MODEL SH5006
K
04
2889
DYNAMOMETER - MODEL FCE AND MODEL MSC
K
01
2492
KADANCE 2000
K
98
1730
DIGIT-GRIP WITH LCD, MODEL NUMBER DGR 002
K
98
0363
ORO-FACIAL MYOGRAPHIC MEASUREMENT INSTRUMENT (OMMI)
K
96
4933
MEKANIKA'S SPINAL STIFFNESS GAUGE (SSG)
K
96
4685
DYNAMOMETER
K
93
5757
GREENLEAF EVAL SYSTEM/ GREENLEAF SOLOSYSTEM
Show All 36 Submissions
NKI
Goniometer With Electrodes
Miscellaneous
Neurological Diagnostic Devices
Neurological Surgical Devices
Neurological Therapeutic Devices
Physical Medicine Diagnostic Devices
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
/
diagnostic-devices
/
LBB
/
K981730
View Source
DIGIT-GRIP WITH LCD, MODEL NUMBER DGR 002
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981730
510(k) Type
Traditional
Applicant
NK BIOTECHNICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/1998
Days to Decision
63 days
Submission Type
Statement