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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Endoscopic Magnetic Retriever
510(k) Number K843135
Device Name BRIMFIELD CANNULATED MAGNETIC RETRIEVER
Applicant
BRIMFIELD SCIENTIFIC INSTRUMENTS
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
BRIMFIELD SCIENTIFIC INSTRUMENTS
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number876.1500
Classification Product Code
FCC  
Date Received08/09/1984
Decision Date 09/26/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
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