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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Attachment, Precision, All
510(k) Number K855167
Device Name DYNA SYSTEM
Applicant
Parker Laboratories, Inc.
155 Schmitt Blvd.
P.O. Box S
Farmingdale,  NY  11735
Applicant Contact NELSON J GENDUSA
Correspondent
Parker Laboratories, Inc.
155 Schmitt Blvd.
P.O. Box S
Farmingdale,  NY  11735
Correspondent Contact NELSON J GENDUSA
Regulation Number872.3165
Classification Product Code
EGG  
Date Received12/26/1985
Decision Date 03/04/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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