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510K-Shield-FDA-Certified-PR-2000x1111px-v2

Por 11 de março de 2021

The FDA has cleared Zymo Research’s DNA/RNA Shield™ Collection Tube as a Class II medical device. The FDA’s 510(k) clearance allows the product to be used as an In-vitro Diagnostic (IVD) device for COVID-19 testing.

Author PR Newswire

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