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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K891023
Device Name SIEMENS CEILING STAND 800F, 800 AND 810
Applicant
Siemens Medical Electronics
16 Electronics Ave.
Danvers,  MA  01923
Applicant Contact MURFITT, PHD
Correspondent
Siemens Medical Electronics
16 Electronics Ave.
Danvers,  MA  01923
Correspondent Contact MURFITT, PHD
Classification Product Code
LDQ
Date Received02/28/1989
Decision Date 07/25/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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