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FDA 510(k)

QUIKCLOT NOSEBLEED

K-Number: K080247 · 2008-02-27

ApplicantZ-Medica Corporation
Decision Date2008-02-27
Product CodeLYA
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

QUIKCLOT NOSEBLEED is the device name listed in this FDA 510(k) record. The listed applicant is Z-Medica Corporation. It received FDA 510(k) clearance on 2008-02-27 under 510(k) number K080247. The device is classified under product code LYA. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUIKCLOT NOSEBLEED?

QUIKCLOT NOSEBLEED is a medical device that received FDA 510(k) clearance on 2008-02-27. The listed applicant is Z-Medica Corporation. The 510(k) number is K080247.

When did QUIKCLOT NOSEBLEED receive FDA 510(k) clearance?

QUIKCLOT NOSEBLEED received FDA 510(k) clearance on 2008-02-27, under 510(k) number K080247.

Who is the listed applicant for QUIKCLOT NOSEBLEED?

The FDA 510(k) record lists Z-Medica Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUIKCLOT NOSEBLEED?

The FDA product code for QUIKCLOT NOSEBLEED is LYA.

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Other records listing Z-Medica Corporation 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.

K120782INTERVENTIONAL HEMOSTATIC BANDAGEK090620QUIKCLOT INTEVENTIONAL, MODEL P/N 182K072474QUIKCLOT EXK070010QUIKCLOT SPORT AND QUIKCLOT SPORT SILVERK061767QUIKCLOT 1ST RESPONSE & QUIKCLOT ACS+K051955QUICKCLOT ACS - ACCELERATED CLOTTING SPONGE

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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.

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