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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Laryngoscope, Rigid
510(k) Number K922275
Device Name UPSHERSCOPE(TM)
Applicant
Upsher Laryngoscope Co.
1155c Chess Dr., Suite A
P.O. Box 4519
Foster City,  CA  94404
Applicant Contact MICHAEL UPSHER
Correspondent
Upsher Laryngoscope Co.
1155c Chess Dr., Suite A
P.O. Box 4519
Foster City,  CA  94404
Correspondent Contact MICHAEL UPSHER
Regulation Number868.5540
Classification Product Code
CCW  
Date Received05/14/1992
Decision Date 01/06/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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