Anesthesiology
Review Panel
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- ChemistryReview Panel
- DentalReview Panel
- Ear, Nose, ThroatReview Panel
- Gastroenterology and UrologyReview Panel
- General HospitalReview Panel
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- Cardiovascular Diagnostic DevicesCFR Sub-Part
- Cardiovascular Monitoring DevicesCFR Sub-Part
- Cardiovascular Therapeutic DevicesCFR Sub-Part
- Diagnostic DevicesCFR Sub-Part
- PDQNeurosurgical Nerve Locator2Product Code
- HRWDynamometer, Nonpowered1Product Code
- KQWGoniometer, Nonpowered1Product Code
- KQXGoniometer, Ac-Powered1Product Code
- LBBDynamometer, Ac-Powered2Product Code
- K162412Hoggan Scientific® microFET2™2Cleared 510(K)
- K073154FACTS HAND AND PINCH GRIP COMBO2Cleared 510(K)
- K052309DIGITAL HAND DYNAMOMETER, MODEL SH5003; DIGITAL PINCH GAUGE, MODEL SH50062Cleared 510(K)
- K042889DYNAMOMETER - MODEL FCE AND MODEL MSC2Cleared 510(K)
- K012492KADANCE 20002Cleared 510(K)
- K981730DIGIT-GRIP WITH LCD, MODEL NUMBER DGR 0022Cleared 510(K)
- K980363ORO-FACIAL MYOGRAPHIC MEASUREMENT INSTRUMENT (OMMI)2Cleared 510(K)
- K964933MEKANIKA'S SPINAL STIFFNESS GAUGE (SSG)2Cleared 510(K)
- K964685DYNAMOMETER2Cleared 510(K)
- K935757GREENLEAF EVAL SYSTEM/ GREENLEAF SOLOSYSTEM2Cleared 510(K)
- K931321CSD 200/300/400/500 DYNAMOMETER2Cleared 510(K)
- K923964NK GRASP SENSOR, MODEL GA0012Cleared 510(K)
- K923965NK GRASP SENSOR, MODEL GA0022Cleared 510(K)
- K923963NK DIGI-GRIP SENSOR, MODEL DGR0012Cleared 510(K)
- K923262DMG100 AND 500 ISOMETRIC STRENGTH DYNAMOMETER2Cleared 510(K)
- K922029REMUSK MP2Cleared 510(K)
- K922940CLINCAL HAND MASTER SYSTEM MODEL # EXH9000-0022Cleared 510(K)
- K921268NK DYNA-GRIP SENSOR, MODEL DG0012Cleared 510(K)
- K920183TECH DYNE - HP-2000, SKREEN TEST, RMS-2002Cleared 510(K)
- K914436CLINICAL HANDMASTER SYSTEM OR CHMS2Cleared 510(K)
- K914059NK DEVIATION SENSOR, MODEL DV0012Cleared 510(K)
- K914054NK GRASP SENSOR, MODEL GR0012Cleared 510(K)
- K914055PINCH SENSOR, MODEL PF0012Cleared 510(K)
- K914056NK PINCH SENSOR, MODEL PF0022Cleared 510(K)
- K914057NK PINCH SENSOR, MODEL PA0012Cleared 510(K)
- K914058NK PINCH SENSOR, MODEL PA0022Cleared 510(K)
- K912526GS-220 HAND IMPAIRMENT EVALUATION SYSTEM2Cleared 510(K)
- K901290ELECTRO-GONIOMETER DIAGNOSTIC DEVICE2Cleared 510(K)
- K893537GREENLEAF HAND IMPAIRMENT EVALUATION SYSTEM2Cleared 510(K)
- K884165MUSCLE EXAMINATION & EXERCISE DOSIMETER (MEED) SYS2Cleared 510(K)
- K881388KIN-COM JR2Cleared 510(K)
- K880464DYNATRON II2Cleared 510(K)
- K860226FORCE EVALUATION AND TESTING SYSTEM (FETS)2Cleared 510(K)
- K850697DIGITAL GRIP/PINCH STRENGTH METOR2Cleared 510(K)
- K812899MED-EX2Cleared 510(K)
- K811312MYO-METRIC II2Cleared 510(K)
- NKIGoniometer With Electrodes2Product Code
- MiscellaneousMiscellaneous
- Neurological Diagnostic DevicesCFR Sub-Part
- Neurological Surgical DevicesCFR Sub-Part
- Neurological Therapeutic DevicesCFR Sub-Part
- Physical Medicine Diagnostic DevicesCFR Sub-Part
- Physical Medicine Prosthetic DevicesCFR Sub-Part
- Physical Medicine Therapeutic DevicesCFR Sub-Part
- Surgical DevicesCFR Sub-Part
- Therapeutic DevicesCFR Sub-Part
- Obstetrical and GynecologicalReview Panel
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NK PINCH SENSOR, MODEL PA002
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K914058
- 510(k) Type
- Traditional
- Applicant
- NK BIOTECHNICAL ENGINEERING CO.
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 12/6/1991
- Days to Decision
- 87 days
- Submission Type
- Statement