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Neothermia Corporation

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K052246 MODIFICATION TO EN-BLOC BIOPSY SYSTEMGEI2005-08-22 View
510(k) K050737 NEOTHERMIA EN-BLOC BIOPSY SYSTEMGEI2005-03-31 View
510(k) K042170 EN-BLOC BIOPSY SYSTEM MODEL#777-110,777-001,777-002,777-006,777-301,777-302,777-115,777-120GEI2004-09-07 View
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