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FDA 510(k)

BLOODSTOP HEMOSTATIC GAUZE; IX HEMOSTATIC GAUZE

K-Number: K072681 · 2007-11-02

Decision Date2007-11-02
Product CodeQSY
DecisionSubstantially Equivalent

Device Summary

BLOODSTOP HEMOSTATIC GAUZE; IX HEMOSTATIC GAUZE is the device name listed in this FDA 510(k) record. The listed applicant is Lifescience Plus, Inc.. It received FDA 510(k) clearance on 2007-11-02 under 510(k) number K072681. The device is classified under product code QSY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOODSTOP HEMOSTATIC GAUZE; IX HEMOSTATIC GAUZE?

BLOODSTOP HEMOSTATIC GAUZE; IX HEMOSTATIC GAUZE is a medical device that received FDA 510(k) clearance on 2007-11-02. The listed applicant is Lifescience Plus, Inc.. The 510(k) number is K072681.

When did BLOODSTOP HEMOSTATIC GAUZE; IX HEMOSTATIC GAUZE receive FDA 510(k) clearance?

BLOODSTOP HEMOSTATIC GAUZE; IX HEMOSTATIC GAUZE received FDA 510(k) clearance on 2007-11-02, under 510(k) number K072681.

Who is the listed applicant for BLOODSTOP HEMOSTATIC GAUZE; IX HEMOSTATIC GAUZE?

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

What is the FDA product code for BLOODSTOP HEMOSTATIC GAUZE; IX HEMOSTATIC GAUZE?

The FDA product code for BLOODSTOP HEMOSTATIC GAUZE; IX HEMOSTATIC GAUZE is QSY.

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 Lifescience Plus, 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: QSY)

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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