HEMO-NATE L-P KIT
K-Number: K821814 · 1982-07-09
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Device Summary
Frequently Asked Questions
What is the HEMO-NATE L-P KIT?
HEMO-NATE L-P KIT is a medical device that received FDA 510(k) clearance on 1982-07-09. The listed applicant is Int'L Corp.. The 510(k) number is K821814.
When did HEMO-NATE L-P KIT receive FDA 510(k) clearance?
HEMO-NATE L-P KIT received FDA 510(k) clearance on 1982-07-09, under 510(k) number K821814.
Who is the listed applicant for HEMO-NATE L-P KIT?
The FDA 510(k) record lists Int'L Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEMO-NATE L-P KIT?
The FDA product code for HEMO-NATE L-P KIT is KDD.
Other records listing Int'L Corp. 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: KDD)
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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