FDA 510(k) Application Details - K971045

Device Classification Name Thermometer, Electronic, Clinical

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510(K) Number K971045
Device Name Thermometer, Electronic, Clinical
Applicant POLYMEDICA INDUSTRIES, INC.
581 CONFERENCE PL.
GOLDEN, CO 80401 US
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Contact SUSAN COLLINS
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Regulation Number 880.2910

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Classification Product Code FLL
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Date Received 03/21/1997
Decision Date 05/02/1997
Decision SESE - SUBST EQUIV
Classification Advisory Committee HO - General Hospital
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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