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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Sterilizer, Dry Heat
510(k) Number K871615
Device Name U. V. GERMICIDAL UNIT
Applicant
Lorvic Corp.
8810 Frost Ave.
St. Louis,  MO  63134
Applicant Contact JOHN M BARRETT
Correspondent
Lorvic Corp.
8810 Frost Ave.
St. Louis,  MO  63134
Correspondent Contact JOHN M BARRETT
Regulation Number880.6870
Classification Product Code
KMH  
Date Received04/27/1987
Decision Date 09/11/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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