ERIKA HEPARIN INFUSION ADAPTOR
K-Number: K810824 · 1981-04-17
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Device Summary
Frequently Asked Questions
What is the ERIKA HEPARIN INFUSION ADAPTOR?
ERIKA HEPARIN INFUSION ADAPTOR is a medical device that received FDA 510(k) clearance on 1981-04-17. The listed applicant is Erika, Inc.. The 510(k) number is K810824.
When did ERIKA HEPARIN INFUSION ADAPTOR receive FDA 510(k) clearance?
ERIKA HEPARIN INFUSION ADAPTOR received FDA 510(k) clearance on 1981-04-17, under 510(k) number K810824.
Who is the listed applicant for ERIKA HEPARIN INFUSION ADAPTOR?
The FDA 510(k) record lists Erika, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ERIKA HEPARIN INFUSION ADAPTOR?
The FDA product code for ERIKA HEPARIN INFUSION ADAPTOR is FJK.
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 Erika, 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: FJK)
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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