HEMO-DIAL
K-Number: K832866 · 1983-11-03
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Device Summary
Frequently Asked Questions
What is the HEMO-DIAL?
HEMO-DIAL is a medical device that received FDA 510(k) clearance on 1983-11-03. The listed applicant is Cmi Pharmaceuticals, Inc.. The 510(k) number is K832866.
When did HEMO-DIAL receive FDA 510(k) clearance?
HEMO-DIAL received FDA 510(k) clearance on 1983-11-03, under 510(k) number K832866.
Who is the listed applicant for HEMO-DIAL?
The FDA 510(k) record lists Cmi Pharmaceuticals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEMO-DIAL?
The FDA product code for HEMO-DIAL is KPO.
Related Devices (Code: KPO)
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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