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)

ASI DEIONIZER & CARBON EXCHANGE SERVICE FOR HEMODIALYSIS

K-Number: K102892 · 2011-02-03

Decision Date2011-02-03
Product CodeFIP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ASI DEIONIZER & CARBON EXCHANGE SERVICE FOR HEMODIALYSIS is the device name listed in this FDA 510(k) record. The listed applicant is Aqua Sciences, Inc.. It received FDA 510(k) clearance on 2011-02-03 under 510(k) number K102892. The device is classified under product code FIP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASI DEIONIZER & CARBON EXCHANGE SERVICE FOR HEMODIALYSIS?

ASI DEIONIZER & CARBON EXCHANGE SERVICE FOR HEMODIALYSIS is a medical device that received FDA 510(k) clearance on 2011-02-03. The listed applicant is Aqua Sciences, Inc.. The 510(k) number is K102892.

When did ASI DEIONIZER & CARBON EXCHANGE SERVICE FOR HEMODIALYSIS receive FDA 510(k) clearance?

ASI DEIONIZER & CARBON EXCHANGE SERVICE FOR HEMODIALYSIS received FDA 510(k) clearance on 2011-02-03, under 510(k) number K102892.

Who is the listed applicant for ASI DEIONIZER & CARBON EXCHANGE SERVICE FOR HEMODIALYSIS?

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

What is the FDA product code for ASI DEIONIZER & CARBON EXCHANGE SERVICE FOR HEMODIALYSIS?

The FDA product code for ASI DEIONIZER & CARBON EXCHANGE SERVICE FOR HEMODIALYSIS is FIP.

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.

Related Devices (Code: FIP)

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.

↑