PRINCETON, N.J., Jan. 19 Abbott announced todaythat the U.S. Food and Drug Administration (FDA) has granted waived statusunder the Clinical Laboratory Improvement Amendments of 1988 (CLIA) for ...

Abbott Laboratories, Inc. ABT recently announced the receipt of the FDA approval for the i-STAT TBI (traumatic brain injury) cartridge. The test runs on Abbott's portable i-STAT Alinity instrument, ...

Abbott Laboratories (NYSE:ABT) said that it has received FDA clearance for its i-STAT TBI test cartridge to be used with whole blood in the evaluation of patients with suspected concussions, allowing ...

The test can be used to evaluate patients up to 24 hours after injury. The Food and Drug Administration (FDA) has cleared the i-STAT ® TBI cartridge for use with whole blood to aid in the evaluation ...

The inclusion criteria were as follows: Patients: patients presenting at emergency departments. Intervention: the CG4+ and CHEM8+ cartridges using the i‑STAT analyser for blood test (manufactured by ...

PANAJI: The Government of Goa and M/s. Colorcon Asian Pvt Ltd, signed and exchanged Memorandum of Understanding (MoU) regarding the supply of i-STAT cartridges and machines for the use of various ...

The CHEM 8+ cartridge is designed for use with the i-STAT, a market-leading automated hand-held blood analyzer that performs a comprehensive panel of critical tests at the patient's bedside in only a ...

Co announces that the FDA has granted waived status under the Clinical Laboratory Improvement Amendements of 1988 for its handheld i-STAT CHEM8+ test cartridge, making it more widely available for use ...

The use of i‑STAT is not currently planned into any NICE guidance programme. NICE has issued the following relevant guidance which includes recommendations for physiological measurement (including ...