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Fischer Imaging Corporation

11 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
SenoScan Full Field Digital Mammography System--Product Number 94001G-3, 105200G recall (Z-0757-06)Fischer Imaging Corporation2006-04-11
Electrophysiology Imaging System recall (Z-1524-05)Fischer Imaging Corporation2005-09-09
Electrophysiology Imaging System recall (Z-1525-05)Fischer Imaging Corporation2005-09-09
Electrophysiology Imaging System recall (Z-1526-05)Fischer Imaging Corporation2005-09-09
Electrophysiology Imaging System recall (Z-1527-05)Fischer Imaging Corporation2005-09-09
VersaRad Generator recall (Z-0787-05)Fischer Imaging Corporation2005-05-03
Bloom DTU-215-B Programmable Stimulator recall (Z-0713-05)Fischer Imaging Corporation2005-04-19
MammoTest Breast Biopsy System. recall (Z-0379-05)Fischer Imaging Corporation2005-01-05
SenoScan True View Digital Mammography System recall (Z-0939-04)Fischer Imaging Corporation2004-07-20
VersaRad/Traumex General Radiographic System. recall (Z-0974-04)Fischer Imaging Corporation2004-07-20
Fischer SenoScan True View Digital Mammography System. recall (Z-1094-04)Fischer Imaging Corporation2004-07-20

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Every clearance here is in the API, with alerts when new ones post.