FDA 510(k) Application Details - K771847

Device Classification Name Esthesiometer

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510(K) Number K771847
Device Name Esthesiometer
Applicant JABLECKI, CHARLES, DR.

, US
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Regulation Number 882.1500

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Classification Product Code GXB
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Date Received 09/28/1977
Decision Date 11/02/1977
Decision SE - Substantially Equivalent
Classification Advisory Committee CH - Clinical Chemistry
Review Advisory Committee NE - Neurology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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