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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name cannula, nasal, oxygen
510(k) Number K760080
Device Name CANNULA, NASAL, FOR OXYGEN
Applicant
INSPIRON CORP.
803 N. Front St. Suite 3
mchenry,  IL  60050
Correspondent
INSPIRON CORP.
803 N. Front St. Suite 3
mchenry,  IL  60050
Regulation Number868.5340
Classification Product Code
CAT  
Date Received06/21/1976
Decision Date 07/15/1976
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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