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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Splint, Nasal
510(k) Number K890599
Device Name HOOD NASAL SPLINT
Applicant
Hood Laboratories
575 Washington St.
Pembroke,  MA  02359
Applicant Contact LEWIS H MARTEN
Correspondent
Hood Laboratories
575 Washington St.
Pembroke,  MA  02359
Correspondent Contact LEWIS H MARTEN
Regulation Number874.5800
Classification Product Code
EPP  
Date Received02/06/1989
Decision Date 03/17/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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