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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stylet, Tracheal Tube
510(k) Number K770374
Device Name STYLETTE, SLICK, CAT. NO. 2000B
Applicant
Medical Products Div. P.O.L.A. Plasti
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Medical Products Div. P.O.L.A. Plasti
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number868.5790
Classification Product Code
BSR  
Date Received02/25/1977
Decision Date 03/30/1977
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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