Intersect Systems, Inc.
Intersect Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1983, most recent 2002.
Top product codes for Intersect Systems, Inc.
Recent clearances by Intersect Systems, Inc.
- K021636 — ALBUMIN REAGENT
- K011972 — DIRECT BILIRUBIN REAGENT
- K011692 — HOMOGENEOUS ENZYMIC HOMOCYSTEINE REAGENT
- K003892 — TOTAL BILIRUBIN REAGENT
- K983937 — DUAL VIAL CREATININE REAGENT
- K974833 — CK-NAC REAGENT
- K941807 — INTERSECT SYSTEMS' NON-MERCURIC CHLORIDE REAGENT
- K932888 — INTERSECT SYSTEMS DIRECT AMYLASE REAGENT
- K934039 — INTERSECT SYSTEMS HDL CHOLESTEROL REAGENT SET
- K932267 — ENZYMATIC CO2 REAGENT, MODIFICATION
- K913225 — URINE/CSF MICROPROTEIN REAGENT
- K911297 — CHLORIDE REAGENT
- K881169 — CARBON DIOXIDE REAGENT
- K873835 — GLUCOSE-HK REAGENT
- K871979 — GAMMA GLUTAMYLTRANSFERASE REAGENT
- K870827 — INTERSECT SYSTEMS TRIGLYCERIDE-GPO REAGENT
- K870828 — INTERSECT SYSTEMS ENZYMATIC CHOLESTEROL REAGENT
- K870616 — GLUCOSE OXIDASE REAGENT
- K841148 — MINI PECG-MODIFICATION
- K832882 — DIF-STET
- K832883 — MINI-PECG
Data sourced from openFDA. This site is unofficial and independent of the FDA.