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FDA 510(k)

HESUNG BLOOD TRANSFUSION SETS

K-Number: K841562 · 1984-07-23

Decision Date1984-07-23
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HESUNG BLOOD TRANSFUSION SETS is the device name listed in this FDA 510(k) record. The listed applicant is Amkor Trading Co.. It received FDA 510(k) clearance on 1984-07-23 under 510(k) number K841562. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HESUNG BLOOD TRANSFUSION SETS?

HESUNG BLOOD TRANSFUSION SETS is a medical device that received FDA 510(k) clearance on 1984-07-23. The listed applicant is Amkor Trading Co.. The 510(k) number is K841562.

When did HESUNG BLOOD TRANSFUSION SETS receive FDA 510(k) clearance?

HESUNG BLOOD TRANSFUSION SETS received FDA 510(k) clearance on 1984-07-23, under 510(k) number K841562.

Who is the listed applicant for HESUNG BLOOD TRANSFUSION SETS?

The FDA 510(k) record lists Amkor Trading Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HESUNG BLOOD TRANSFUSION SETS?

The FDA product code for HESUNG BLOOD TRANSFUSION SETS is FPA.

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 Amkor Trading Co. 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: FPA)

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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