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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Pump, Portable, Aspiration (Manual Or Powered)
510(k) Number K952632
Device Name S-SCORT
Applicant
Sscor
11064 Randall St.
Sun Valley,  CA  91352
Applicant Contact SAM L SAY
Correspondent
Sscor
11064 Randall St.
Sun Valley,  CA  91352
Correspondent Contact SAM L SAY
Regulation Number878.4780
Classification Product Code
BTA  
Date Received06/08/1995
Decision Date 06/16/1995
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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