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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Apparatus, Suction, Ward Use, Portable, Ac-Powered
510(k) Number K930852
Device Name OLYMPUS SUCTION PUMP MODEL KV-4
Applicant
Keymed (Medical & Industrial Equipment), Ltd.
Keymed House,Stock Rd.
Southend-On-Sea, Essex Ss2 5qh
Essex,  GB
Applicant Contact ROGER GRAY
Correspondent
Keymed (Medical & Industrial Equipment), Ltd.
Keymed House,Stock Rd.
Southend-On-Sea, Essex Ss2 5qh
Essex,  GB
Correspondent Contact ROGER GRAY
Regulation Number878.4780
Classification Product Code
JCX  
Date Received02/18/1993
Decision Date 03/31/1994
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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