SIEMENS ANGIOTRON

Synchronizer, Ecg / Respirator, Radiographic

SIEMENS CORP.

The following data is part of a premarket notification filed by Siemens Corp. with the FDA for Siemens Angiotron.

Pre-market Notification Details

Device IDK811587
510k NumberK811587
Device Name:SIEMENS ANGIOTRON
ClassificationSynchronizer, Ecg / Respirator, Radiographic
Applicant SIEMENS CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeIXO  
CFR Regulation Number892.1970 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1981-06-05
Decision Date1981-07-10

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