Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BICARD MIXING SYSTEM

K-Number: K030366 · 2004-04-19

Decision Date2004-04-19
Product CodeFIN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BICARD MIXING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Dialysis Systems, Inc.. It received FDA 510(k) clearance on 2004-04-19 under 510(k) number K030366. The device is classified under product code FIN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BICARD MIXING SYSTEM?

BICARD MIXING SYSTEM is a medical device that received FDA 510(k) clearance on 2004-04-19. The listed applicant is Dialysis Systems, Inc.. The 510(k) number is K030366.

When did BICARD MIXING SYSTEM receive FDA 510(k) clearance?

BICARD MIXING SYSTEM received FDA 510(k) clearance on 2004-04-19, under 510(k) number K030366.

Who is the listed applicant for BICARD MIXING SYSTEM?

The FDA 510(k) record lists Dialysis Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BICARD MIXING SYSTEM?

The FDA product code for BICARD MIXING SYSTEM is FIN.

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 Dialysis Systems, 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: FIN)

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.

↑