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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Probe
510(k) Number K800729
Device Name PROBE
Applicant
STAINLESS MFG., INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
STAINLESS MFG., INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number888.4540
Classification Product Code
HXB  
Date Received04/01/1980
Decision Date 04/08/1980
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Type Traditional
Reviewed by Third Party No
Combination Product No
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