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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K861695
Device Name SURGICAL PLASTERS
Applicant
Salvaplast Industries
Kiryat Matalon
Petach-Tiqva
49 348, Israel,  IL
Applicant Contact LANDAU
Correspondent
Salvaplast Industries
Kiryat Matalon
Petach-Tiqva
49 348, Israel,  IL
Correspondent Contact LANDAU
Date Received05/02/1986
Decision Date 08/01/1986
Decision Substantially Equivalent (SESE)
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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