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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name circuit, breathing (w connector, adaptor, y piece)
510(k) Number K940890
Device Name CORRUGATED TUBING
Applicant
CLEVELAND TUBING, INC.
1675 HARDEMAN LN.
P.O. BOX 2698
CLEVELAND,  TN  37320
Applicant Contact ROBERT STEINBARGER
Correspondent
CLEVELAND TUBING, INC.
1675 HARDEMAN LN.
P.O. BOX 2698
CLEVELAND,  TN  37320
Correspondent Contact ROBERT STEINBARGER
Regulation Number868.5240
Classification Product Code
CAI  
Date Received01/25/1994
Decision Date 11/10/1994
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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