Quantra Hemostasis Analyzer
K-Number: K230461 · 2023-03-24
Device Summary
Frequently Asked Questions
What is the Quantra Hemostasis Analyzer?
Quantra Hemostasis Analyzer is a medical device that received FDA 510(k) clearance on 2023-03-24. The listed applicant is Hemosonics, LLC. The 510(k) number is K230461.
When did Quantra Hemostasis Analyzer receive FDA 510(k) clearance?
Quantra Hemostasis Analyzer received FDA 510(k) clearance on 2023-03-24, under 510(k) number K230461.
Who is the listed applicant for Quantra Hemostasis Analyzer?
The FDA 510(k) record lists Hemosonics, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Quantra Hemostasis Analyzer?
The FDA product code for Quantra Hemostasis Analyzer is QFR.
Other records listing Hemosonics, LLC as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: QFR)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.