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The DU Pont Co.

FDA 510(k) & PMA Approved Devices — 13 products

Total Devices13
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K953475 CDS COMPACT DAYLIGHT CASSETTE FOR VIDEO IMAGINGLMC1995-10-07 View
510(k) K953477 MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGINGLMC1995-10-07 View
510(k) K952891 CRONEX LOW ABSORPTION CASSETTEIXA1995-07-13 View
510(k) K945125 DUPONT ACA VANCOMYCIN (VANC) METHODLEH1995-03-10 View
510(k) K943704 LIPASE CALIBRATORJIT1994-09-14 View
510(k) K900492 LABELING CHANGE - VIASPAN(TM) (BELZER UW)KDL1990-03-20 View
510(k) K885259 ACA THYRONINE UPTAKE (TU E) METHODKHQ1989-02-17 View
510(k) K885258 ACA THYROXINE (T4 E) METHODKLI1989-02-17 View
510(k) K884700 ANALYST THYROXINE (T4) ROTORKLI1989-01-27 View
510(k) K884169 DU PONT ANALYST THYROID ROTORCEL1989-01-24 View
510(k) K884168 ANALYST THYROXINE (T4) & THYRONINE UPTAKE CALIBRA.JIS1988-11-29 View
510(k) K884170 ANALYST THEOPHYLLINE CALIBRATORDLJ1988-11-16 View
510(k) K884002 ANALYST THEOPHYLLINE ROTORKLS1988-10-31 View
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