HORSE BLOOD CELLS IN ALSEVERS CITRATE/DEFIBRINATED
K-Number: K861817 · 1986-05-20
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Device Summary
Frequently Asked Questions
What is the HORSE BLOOD CELLS IN ALSEVERS CITRATE/DEFIBRINATED?
HORSE BLOOD CELLS IN ALSEVERS CITRATE/DEFIBRINATED is a medical device that received FDA 510(k) clearance on 1986-05-20. The listed applicant is Hazleton Research Products, Inc.. The 510(k) number is K861817.
When did HORSE BLOOD CELLS IN ALSEVERS CITRATE/DEFIBRINATED receive FDA 510(k) clearance?
HORSE BLOOD CELLS IN ALSEVERS CITRATE/DEFIBRINATED received FDA 510(k) clearance on 1986-05-20, under 510(k) number K861817.
Who is the listed applicant for HORSE BLOOD CELLS IN ALSEVERS CITRATE/DEFIBRINATED?
The FDA 510(k) record lists Hazleton Research Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HORSE BLOOD CELLS IN ALSEVERS CITRATE/DEFIBRINATED?
The FDA product code for HORSE BLOOD CELLS IN ALSEVERS CITRATE/DEFIBRINATED is KIS.
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 Hazleton Research Products, 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: KIS)
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
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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