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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name tubes, gastrointestinal (and accessories)
510(k) Number K922209
Device Name NASOGRASTRIC TUBBE HOLDER
Applicant
INNOVATIVE MEDICAL DESIGN CORP.
1322 ROBIN LN.
BAYSIDE,  NY  11360
Applicant Contact HENRY J ALLETTO
Correspondent
INNOVATIVE MEDICAL DESIGN CORP.
1322 ROBIN LN.
BAYSIDE,  NY  11360
Correspondent Contact HENRY J ALLETTO
Regulation Number876.5980
Classification Product Code
KNT  
Date Received05/12/1992
Decision Date 10/30/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
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