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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Syringe, Piston
510(k) Number K781154
Device Name SYRINGE, INSULIN, HYPOTIP
Applicant
NATIONAL PATENT DEVELOPMENT CORP.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
NATIONAL PATENT DEVELOPMENT CORP.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number880.5860
Classification Product Code
FMF  
Date Received07/10/1978
Decision Date 08/10/1978
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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