LIAISON N-TACT PTH CALIBRATION VERIFIERS MODEL 310913
K-Number: K093498 · 2009-12-14
Advertisement
Device Summary
Frequently Asked Questions
What is the LIAISON N-TACT PTH CALIBRATION VERIFIERS MODEL 310913?
LIAISON N-TACT PTH CALIBRATION VERIFIERS MODEL 310913 is a medical device that received FDA 510(k) clearance on 2009-12-14. The listed applicant is DiaSorin, Inc.. The 510(k) number is K093498.
When did LIAISON N-TACT PTH CALIBRATION VERIFIERS MODEL 310913 receive FDA 510(k) clearance?
LIAISON N-TACT PTH CALIBRATION VERIFIERS MODEL 310913 received FDA 510(k) clearance on 2009-12-14, under 510(k) number K093498.
Who is the listed applicant for LIAISON N-TACT PTH CALIBRATION VERIFIERS MODEL 310913?
The FDA 510(k) record lists DiaSorin, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIAISON N-TACT PTH CALIBRATION VERIFIERS MODEL 310913?
The FDA product code for LIAISON N-TACT PTH CALIBRATION VERIFIERS MODEL 310913 is JJX.
Related Clinical Trials
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.
Other records listing DiaSorin, Inc. 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: JJX)
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.
Advertisement