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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Examination, Medical, Powered
510(k) Number K845023
Device Name STORZ PLASTIC SURGERY & EXAMINATION LOUNGE 7000
Applicant
Storz Instrument Co.
3365 Tree Ct. Industrial Blvd.
St. Louis,  MO  63122
Applicant Contact TOM GRANT
Correspondent
Storz Instrument Co.
3365 Tree Ct. Industrial Blvd.
St. Louis,  MO  63122
Correspondent Contact TOM GRANT
Regulation Number878.4960
Classification Product Code
LGX  
Date Received12/27/1984
Decision Date 01/28/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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