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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K827371
Device Name CILCO ASCAN
Applicant
Cilco, Inc.
2205 Fifth St. Rd.
P.O. Box 1680
Huntington,  WV  25717
Correspondent
Cilco, Inc.
2205 Fifth St. Rd.
P.O. Box 1680
Huntington,  WV  25717
Date Received03/29/1982
Decision Date 07/09/1982
Decision Substantially Equivalent (SESE)
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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