Anesthesiology
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- Cardiovascular Diagnostic DevicesCFR Sub-Part
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- PDQNeurosurgical Nerve Locator2Product Code
- HRWDynamometer, Nonpowered1Product Code
- K971407JTECH COMMANDER AND ALGOMETER1Cleared 510(K)
- K970870DIGIT-GRIP WITH LCD (DGR002)1Cleared 510(K)
- K894557LIGHTSCOPE SET1Cleared 510(K)
- K861396HANDHELD DYNAMOMETER, MODEL #160 AND #1111Cleared 510(K)
- K821631PINCH GAUGE, 0-301 LBS.1Cleared 510(K)
- K812343PINCH METER1Cleared 510(K)
- K801719BK-7531 PAIN THRESHOLD/FINGER FORCE GAUG1Cleared 510(K)
- K791021MUSCLE TESTING GUN1Cleared 510(K)
- K790302PRESSURE MONITOR, MODEL 2121Cleared 510(K)
- K772415DYNAMETER 50 LB.1Cleared 510(K)
- Show All 12 Submissions
- KQWGoniometer, Nonpowered1Product Code
- KQXGoniometer, Ac-Powered1Product Code
- LBBDynamometer, Ac-Powered2Product Code
- 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
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PINCH GAUGE, 0-301 LBS.
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K821631
- 510(k) Type
- Traditional
- Applicant
- FRED SAMMONS, INC.
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 6/11/1982
- Days to Decision
- 8 days