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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
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