FDA 510(k) Application Details - K820202

Device Classification Name Transducer, Blood-Pressure, Extravascular

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510(K) Number K820202
Device Name Transducer, Blood-Pressure, Extravascular
Applicant LINTON BIOMED CORP.

, US
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Regulation Number 870.2850

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Classification Product Code DRS
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Date Received 01/26/1982
Decision Date 02/12/1982
Decision SE - Substantially Equivalent
Classification Advisory Committee HO - General Hospital
Review Advisory Committee CV - Cardiovascular
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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