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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 K832773
Device Name SHERI-I-SLIP INTUBATING STYLET
Applicant
SHERIDAN CATHETER CORP.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
SHERIDAN CATHETER CORP.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number868.5790
Classification Product Code
BSR  
Date Received08/16/1983
Decision Date 09/12/1983
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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