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FDA 510(k)

EZ-DETECT VISUAL COLOR TEST FOR BLOOD IN STOOL

K-Number: K850431 · 1985-06-17

Decision Date1985-06-17
Product CodeKHE
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

EZ-DETECT VISUAL COLOR TEST FOR BLOOD IN STOOL is the device name listed in this FDA 510(k) record. The listed applicant is Nms Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 1985-06-17 under 510(k) number K850431. The device is classified under product code KHE. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZ-DETECT VISUAL COLOR TEST FOR BLOOD IN STOOL?

EZ-DETECT VISUAL COLOR TEST FOR BLOOD IN STOOL is a medical device that received FDA 510(k) clearance on 1985-06-17. The listed applicant is Nms Pharmaceuticals, Inc.. The 510(k) number is K850431.

When did EZ-DETECT VISUAL COLOR TEST FOR BLOOD IN STOOL receive FDA 510(k) clearance?

EZ-DETECT VISUAL COLOR TEST FOR BLOOD IN STOOL received FDA 510(k) clearance on 1985-06-17, under 510(k) number K850431.

Who is the listed applicant for EZ-DETECT VISUAL COLOR TEST FOR BLOOD IN STOOL?

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

What is the FDA product code for EZ-DETECT VISUAL COLOR TEST FOR BLOOD IN STOOL?

The FDA product code for EZ-DETECT VISUAL COLOR TEST FOR BLOOD IN STOOL is KHE.

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 Nms Pharmaceuticals, 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.

View all 9 devices →

Related Devices (Code: KHE)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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