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FDA 510(k)

HEMCON BANDAGE OTC; HEMCON CATH/AID

K-Number: K030946 · 2003-06-19

ApplicantHemcon, Inc.
Decision Date2003-06-19
Product CodeQSY
DecisionSubstantially Equivalent

Device Summary

HEMCON BANDAGE OTC; HEMCON CATH/AID is the device name listed in this FDA 510(k) record. The listed applicant is Hemcon, Inc.. It received FDA 510(k) clearance on 2003-06-19 under 510(k) number K030946. The device is classified under product code QSY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMCON BANDAGE OTC; HEMCON CATH/AID?

HEMCON BANDAGE OTC; HEMCON CATH/AID is a medical device that received FDA 510(k) clearance on 2003-06-19. The listed applicant is Hemcon, Inc.. The 510(k) number is K030946.

When did HEMCON BANDAGE OTC; HEMCON CATH/AID receive FDA 510(k) clearance?

HEMCON BANDAGE OTC; HEMCON CATH/AID received FDA 510(k) clearance on 2003-06-19, under 510(k) number K030946.

Who is the listed applicant for HEMCON BANDAGE OTC; HEMCON CATH/AID?

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

What is the FDA product code for HEMCON BANDAGE OTC; HEMCON CATH/AID?

The FDA product code for HEMCON BANDAGE OTC; HEMCON CATH/AID 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 Hemcon, 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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