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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Laryngoscope, Rigid
510(k) Number K912905
Device Name LARYNGOSCOPE
Applicant
ACORN GROUP, INC.
47 QUAIL CT
SUITE 301
WALNUT CREEK,  CA  94596
Applicant Contact JAMES P STOUT
Correspondent
ACORN GROUP, INC.
47 QUAIL CT
SUITE 301
WALNUT CREEK,  CA  94596
Correspondent Contact JAMES P STOUT
Regulation Number868.5540
Classification Product Code
CCW  
Date Received07/02/1991
Decision Date 09/30/1991
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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