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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K861784
Device Name MEDSURG SINGLE USE BASIN SET
Applicant
Medsurg Industries, Inc.
251 Exchange Pl.
Herndon,  VA  20170
Applicant Contact DONNA COLLIER
Correspondent
Medsurg Industries, Inc.
251 Exchange Pl.
Herndon,  VA  20170
Correspondent Contact DONNA COLLIER
Date Received05/08/1986
Decision Date 05/21/1986
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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