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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Catheter And Tip, Suction
510(k) Number K803206
Device Name SUCTION PROBE
Applicant
Bemis Health Care
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Bemis Health Care
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number880.6740
Classification Product Code
JOL  
Date Received12/17/1980
Decision Date 01/21/1981
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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