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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Apparatus, Suction, Operating-Room, Wall Vacuum Powered
510(k) Number K880704
Device Name CERULLO SUCTION REGULATOR
Applicant
Aesculap Instruments Corp.
875 Stanton Rd.
Burlingame,  CA  94010
Applicant Contact MARGRIT DUBACH
Correspondent
Aesculap Instruments Corp.
875 Stanton Rd.
Burlingame,  CA  94010
Correspondent Contact MARGRIT DUBACH
Regulation Number880.6740
Classification Product Code
GCX  
Date Received02/22/1988
Decision Date 03/29/1988
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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