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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name driver, surgical, pin
510(k) Number K780255
Device Name NEEDLE DRIVER
Applicant
SCANLAN INTL., INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
SCANLAN INTL., INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number878.4820
Classification Product Code
GFC  
Date Received02/16/1978
Decision Date 04/18/1978
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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