MICROCOIL 150 DIALYZER
K-Number: K811974 · 1981-09-16
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Device Summary
Frequently Asked Questions
What is the MICROCOIL 150 DIALYZER?
MICROCOIL 150 DIALYZER is a medical device that received FDA 510(k) clearance on 1981-09-16. The listed applicant is Erika, Inc.. The 510(k) number is K811974.
When did MICROCOIL 150 DIALYZER receive FDA 510(k) clearance?
MICROCOIL 150 DIALYZER received FDA 510(k) clearance on 1981-09-16, under 510(k) number K811974.
Who is the listed applicant for MICROCOIL 150 DIALYZER?
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 MICROCOIL 150 DIALYZER?
The FDA product code for MICROCOIL 150 DIALYZER is FHS.
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: FHS)
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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