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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Nasopharyngoscope (Flexible Or Rigid)
510(k) Number K951249
Device Name CITATION SINUSCOPE
Applicant
Citation Medical Corp.
230 Edison Way
Reno,  NV  89502
Applicant Contact ROGER KREIBDBERG
Correspondent
Citation Medical Corp.
230 Edison Way
Reno,  NV  89502
Correspondent Contact ROGER KREIBDBERG
Regulation Number874.4760
Classification Product Code
EOB  
Date Received03/20/1995
Decision Date 04/10/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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