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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Laryngoscope, Nasopharyngoscope
510(k) Number K822525
Device Name LARYNGOSCOPES RIGID
Applicant
KELLEHER CORP.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
KELLEHER CORP.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number874.4760
Classification Product Code
EQN  
Date Received08/23/1982
Decision Date 09/09/1982
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
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