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)

SERVICE DEIONIZATION SYST/DI TANK EXCHANGE PROGRAM

K-Number: K915258 · 1993-07-02

ApplicantAqua-Med Systems, Inc.
Decision Date1993-07-02
Product CodeFIP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SERVICE DEIONIZATION SYST/DI TANK EXCHANGE PROGRAM is the device name listed in this FDA 510(k) record. The listed applicant is Aqua-Med Systems, Inc.. It received FDA 510(k) clearance on 1993-07-02 under 510(k) number K915258. 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 SERVICE DEIONIZATION SYST/DI TANK EXCHANGE PROGRAM?

SERVICE DEIONIZATION SYST/DI TANK EXCHANGE PROGRAM is a medical device that received FDA 510(k) clearance on 1993-07-02. The listed applicant is Aqua-Med Systems, Inc.. The 510(k) number is K915258.

When did SERVICE DEIONIZATION SYST/DI TANK EXCHANGE PROGRAM receive FDA 510(k) clearance?

SERVICE DEIONIZATION SYST/DI TANK EXCHANGE PROGRAM received FDA 510(k) clearance on 1993-07-02, under 510(k) number K915258.

Who is the listed applicant for SERVICE DEIONIZATION SYST/DI TANK EXCHANGE PROGRAM?

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

What is the FDA product code for SERVICE DEIONIZATION SYST/DI TANK EXCHANGE PROGRAM?

The FDA product code for SERVICE DEIONIZATION SYST/DI TANK EXCHANGE PROGRAM 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K250471AquaC UNO HFresenius Medical Care Renal Therapies Group, LLCK251851DIASAFEplusUS (F00013010)Fresenius Medical Care Renal Therapies Group, LLCK252181AquaAFresenius Medical Care North AmericaK250514UPT Series Medical RO Water Treatment SystemSpecialty Water Technologies, Inc.K232953AquaBplus; AquaB LITEFresenius Medical Care Renal Therapies Group, LLCK223479AQUAbase nXB.Braun Medical, Inc.

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.

↑