Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ESENSOR WARFARIN SENSITIVITY SALIVA TEST

K-Number: K110786 · 2011-12-02

Decision Date2011-12-02
Product CodeNSU
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ESENSOR WARFARIN SENSITIVITY SALIVA TEST is the device name listed in this FDA 510(k) record. The listed applicant is GenMark Diagnostics, Inc.. It received FDA 510(k) clearance on 2011-12-02 under 510(k) number K110786. The device is classified under product code NSU. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESENSOR WARFARIN SENSITIVITY SALIVA TEST?

ESENSOR WARFARIN SENSITIVITY SALIVA TEST is a medical device that received FDA 510(k) clearance on 2011-12-02. The listed applicant is GenMark Diagnostics, Inc.. The 510(k) number is K110786.

When did ESENSOR WARFARIN SENSITIVITY SALIVA TEST receive FDA 510(k) clearance?

ESENSOR WARFARIN SENSITIVITY SALIVA TEST received FDA 510(k) clearance on 2011-12-02, under 510(k) number K110786.

Who is the listed applicant for ESENSOR WARFARIN SENSITIVITY SALIVA TEST?

The FDA 510(k) record lists GenMark Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ESENSOR WARFARIN SENSITIVITY SALIVA TEST?

The FDA product code for ESENSOR WARFARIN SENSITIVITY SALIVA TEST is NSU.

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.

Related Devices (Code: NSU)

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.

↑