FDA device listing

PICCOLO PRIMARY HEALTH PANEL

FDA device listing 1389889655 · ZOETIS, INC.

Key facts

Proprietary names PICCOLO PRIMARY HEALTH PANEL
Owner/operator ZOETIS, INC.
Owner/operator number 9000378
Premarket submissions K950164
Product codes CDN, CEK, CEM, CGA, CGX, CHH, CIG, CIJ, CJW, CJY, CKA, CKF
Device names CDN - Urease, Photometric, Urea Nitrogen, CEK - Biuret (Colorimetric), Total Protein, CEM - Electrode, Ion Specific, Potassium, CGA - Glucose Oxidase, Glucose, CGX - Alkaline Picrate, Colorimetry, Creatinine, CHH - Enzymatic Esterase--Oxidase, Cholesterol, CIG - Diazo Colorimetry, Bilirubin, CIJ - Saccharogenic, Amylase, CJW - Bromcresol Purple Dye-Binding, Albumin, CJY - Azo Dye, Calcium, CKA - Nadh Oxidation/Nad Reduction, Alt/Sgpt, CKF - Phenylphosphate, Alkaline Phosphatase Or Isoenzymes
Device class Class I, Class II
Classification regulations (21 CFR) 862.1030, 862.1035, 862.1050, 862.1070, 862.1110, 862.1145, 862.1175, 862.1225, 862.1345, 862.1600, 862.1635, 862.1770
Review panels Clinical Chemistry
Registered establishments ABAXIS, INC.
Establishment registrations 2939693
FEI numbers 2939693
Establishment operations Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • 10–99 UDI devices (GUDID) under the same submission
  • 1–9 Device listings citing the same submission
  • Yes Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

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