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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 K781908
Device Name BREATHING CIRCUIT PRODUCTS, ANESTHESIA
Applicant
HOSPITAK, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
HOSPITAK, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number868.5240
Classification Product Code
CAI  
Date Received11/14/1978
Decision Date 11/27/1978
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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