U. S. Diagnostics, Inc.
FDA 510(k) medical device clearances.
Top product codes for U. S. Diagnostics, Inc.
Recent clearances by U. S. Diagnostics, Inc.
- K110435 — EASYGLUCO PLUS BLOOD GLUCOSE MONITORING SYSTEM
- K082201 — G5 INFINITY BLODO GLUCOSE MONITORING SYSTEM WITH MODEL IGM, 0024A
- K061431 — EASYGLUCO, MODEL IGM-0002 G2
- K051651 — G4, MODEL IGM-0004
- K870596 — PROTHROMBIN TIME TEST
- K870685 — COAGULATION CONTROL, LEVEL I
- K870686 — COAGULATION CONTROL, LEVEL II
- K870687 — COAGULATION CONTROL, LEVEL III
- K871283 — CYANMETHEMOGLOBIN STANDARD
- K870737 — U.S. DIAGNOSTICS LIQUID LD ISOENZYME CONTROL
- K870738 — U.S. DIAGNOSTICS LIQUID CK ISOENZYME CONTROL
- K870683 — LIQUID CHEMISTRY CONTROL, LEVEL II
- K870684 — LIQUID CHEMISTRY CONTROL, LEVEL I
- K870688 — O.O2 M CALCIUM CHLORIDE SOLUTION
- K863980 — U.S. DIAGNOSTICS ALKALINE PHOSPHATASE TEST
- K864081 — U.S. DIAGNOSTICS SERUM CHOLESTEROL TEST
- K864231 — U.S. DIAGNOSTICS ENZYMATIC TRIGLYCERIDE TEST
- K863889 — UREA NITROGEN TEST
- K864119 — URIC ACID TEST
- K862669 — ACTIVATED PARTIAL THROMBOPLASTIN TIME TEST
- K862721 — ENZYMATIC BLOOD GLUCOSE
- K862641 — U.S. DIAGNOSTIC INC. HEMOGLOBIN TEST (DRY PACK)
Data sourced from openFDA. This site is unofficial and independent of the FDA.