ICOR NEONATAL HCH
K-Number: K872371 · 1987-09-04
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Device Summary
Frequently Asked Questions
What is the ICOR NEONATAL HCH?
ICOR NEONATAL HCH is a medical device that received FDA 510(k) clearance on 1987-09-04. The listed applicant is Icor AB. The 510(k) number is K872371.
When did ICOR NEONATAL HCH receive FDA 510(k) clearance?
ICOR NEONATAL HCH received FDA 510(k) clearance on 1987-09-04, under 510(k) number K872371.
Who is the listed applicant for ICOR NEONATAL HCH?
The FDA 510(k) record lists Icor AB as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ICOR NEONATAL HCH?
The FDA product code for ICOR NEONATAL HCH is BYD.
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 Icor AB 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: BYD)
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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