Syntex Corp.
Syntex Corp. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 1992.
Top product codes for Syntex Corp.
Recent clearances by Syntex Corp.
- K920314 — TXIT D.A.U. BARBITURATE ASSAY (MODIFICATION)
- K843593 — SURGIPRESS SURGICAL LOOP
- K780997 — AMALGAM ALLOY
- K780769 — S-100 CT SCANNER
- K780483 — FIBER OPTIC HANDPIECE
- K761331 — OPUS I OPTION - FIBER OPTIC L SYSTEM
- K761330 — SYNTEX SYSTEM 6000
- K761332 — HI-SENSITIVITY MODE OPTION FOR S60-1A
- K761264 — OPTIONS FOR STAR DENTAL OPUS I
- K761033 — COMPUTERIZED TOMOGRAPHY SCANNER
Data sourced from openFDA. This site is unofficial and independent of the FDA.