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FDA 510(k) Application Details - K041755
Device Classification Name
Handpiece, Air-Powered, Dental
More FDA Info for this Device
510(K) Number
K041755
Device Name
Handpiece, Air-Powered, Dental
Applicant
J.R. MEDICAL TECHNOLOGIES, INC.
11874 SOUTH EVELYN CIRCLE
HOUSTON, TX 77071 US
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Contact
J. HARVEY KNAUSS
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Regulation Number
872.4200
More FDA Info for this Regulation Number
Classification Product Code
EFB
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
06/29/2004
Decision Date
10/22/2004
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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