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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 K792520
Device Name ANESTHESIA & HOSPITAL SYRINGE HOLDER
Applicant
Medical Innovations Corp.
4221 Richmond Rd., NW
Walker,  MI  49534
Correspondent
Medical Innovations Corp.
4221 Richmond Rd., NW
Walker,  MI  49534
Regulation Number880.5860
Classification Product Code
FMF  
Date Received12/06/1979
Decision Date 02/07/1980
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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