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Syntex Corp.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K920314 TXIT D.A.U. BARBITURATE ASSAY (MODIFICATION)DIS1992-04-17 View
510(k) K843593 SURGIPRESS SURGICAL LOOPHRQ1984-10-24 View
510(k) K780997 AMALGAM ALLOYEJJ1978-07-27 View
510(k) K780769 S-100 CT SCANNERJAK1978-06-02 View
510(k) K780483 FIBER OPTIC HANDPIECEEFB1978-04-28 View
510(k) K761331 OPUS I OPTION - FIBER OPTIC L SYSTEMEAY1977-01-03 View
510(k) K761332 HI-SENSITIVITY MODE OPTION FOR S60-1AJAK1976-12-30 View
510(k) K761330 SYNTEX SYSTEM 6000JAK1976-12-30 View
510(k) K761264 OPTIONS FOR STAR DENTAL OPUS IDYN1976-12-23 View
510(k) K761033 COMPUTERIZED TOMOGRAPHY SCANNERJAK1976-11-24 View
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