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FDA 510(k)

MICRO-COIL 100 COIL DIALYZER

K-Number: K800723 · 1980-05-14

ApplicantErika, Inc.
Decision Date1980-05-14
Product CodeFHS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MICRO-COIL 100 COIL DIALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Erika, Inc.. It received FDA 510(k) clearance on 1980-05-14 under 510(k) number K800723. The device is classified under product code FHS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-COIL 100 COIL DIALYZER?

MICRO-COIL 100 COIL DIALYZER is a medical device that received FDA 510(k) clearance on 1980-05-14. The listed applicant is Erika, Inc.. The 510(k) number is K800723.

When did MICRO-COIL 100 COIL DIALYZER receive FDA 510(k) clearance?

MICRO-COIL 100 COIL DIALYZER received FDA 510(k) clearance on 1980-05-14, under 510(k) number K800723.

Who is the listed applicant for MICRO-COIL 100 COIL 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 MICRO-COIL 100 COIL DIALYZER?

The FDA product code for MICRO-COIL 100 COIL 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.

View all 43 devices →

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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