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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Instrument, Manual, Surgical, General Use
510(k) Number K921210
Device Name SURGICAL INSTRUMENT STAND
Applicant
Murphy Medical Center
3929 Hwy U
Warrenton,  MO  63383
Applicant Contact PAUL G MURPHY
Correspondent
Murphy Medical Center
3929 Hwy U
Warrenton,  MO  63383
Correspondent Contact PAUL G MURPHY
Regulation Number878.4800
Classification Product Code
MDM  
Date Received03/12/1992
Decision Date 04/29/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
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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