Agilent Technologies, Inc.
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Global Device Approvals Snapshot: 11-17 June 2019
A snapshot of global medical device approvals captured during the past week in Medtech Insight's Approvals Tracker, including a PMA supplement for Agilent’s PD-L1 IHC 22C3 pharmDx companion diagnostic for Merck’s Keytruda (pembrolizumab), an anti-PD-1 drug, for patients with head and neck squamous cell carcinoma. The US FDA also approved a supplement for the Cochlear Nucleus Profile Plus Series Cochlear Implant, designed to be safe with magnetic resonance imaging.
Company Information
- Industry
- Contract Research, Toxicology Testing-CRO
- In Vitro Diagnostics
- Laboratory Testing Services
- Research, Analytical Equipment & Supplies
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Pharmaceuticals
- Chiral Chemistry
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Medical Devices
- Diagnostic Equipment & Supplies
- Other Names / Subsidiaries
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- ACEA Biosciences
- Advanced Analytical Technologies
- BioTek
- Cartagenia
- Dako
- J&W Scientific Inc.
- Lasergen, Inc.
- Luxcel Biosciences
- Multiplicom
- Seahorse Bioscience
- Silicon Genetics
- Ultra Scientific