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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
510(k) Number K080722
Device Name PRIMADO SURGICAL DRILL
Applicant
NAKANISHI, INC.
1425 K STREET, N.W.
SUITE 1100
WASHINGTON,  DC  20005
Applicant Contact KEITH A BARRITT
Correspondent
NAKANISHI, INC.
1425 K STREET, N.W.
SUITE 1100
WASHINGTON,  DC  20005
Correspondent Contact KEITH A BARRITT
Regulation Number874.4250
Classification Product Code
ERL  
Date Received03/13/2008
Decision Date 09/17/2008
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
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