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FDA 510(k)

MODIFIED C-DAK

K-Number: K844185 · 1985-01-03

ApplicantCd Medical, Inc.
Decision Date1985-01-03
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODIFIED C-DAK is the device name listed in this FDA 510(k) record. The listed applicant is Cd Medical, Inc.. It received FDA 510(k) clearance on 1985-01-03 under 510(k) number K844185. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED C-DAK?

MODIFIED C-DAK is a medical device that received FDA 510(k) clearance on 1985-01-03. The listed applicant is Cd Medical, Inc.. The 510(k) number is K844185.

When did MODIFIED C-DAK receive FDA 510(k) clearance?

MODIFIED C-DAK received FDA 510(k) clearance on 1985-01-03, under 510(k) number K844185.

Who is the listed applicant for MODIFIED C-DAK?

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

What is the FDA product code for MODIFIED C-DAK?

The FDA product code for MODIFIED C-DAK is KOC.

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Other records listing Cd Medical, Inc. as applicant

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K925654CD HOME DIALYSERVICE HEMODIALYSIS TRAYK910215DRAKE WILLOCK SYSTEM 1000 DIALYSATE DELIVERY SYSTK901520WURTZ CHOLEY CLIP (TM)K894106DRAKE WILLOCK REVERSE OSMOSIS WATER TREATMENT SYSTK884353ULTRX(TM) 850 ARTIFICIAL KIDNEYK880459480 HIGH-FLOW ULTRAFILTRATION CONTROL DIALYSATE

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Related Devices (Code: KOC)

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.

K242479BLOOD TUBING LINES FOR HEMODIALYSIS AL Series (Archloop) BLOOD TUBING LINES FOR HEMODIALYSIS C18 Series AL-ADC-PU, AL-CDC-PU, C18RDC-PU, C18BDD-PU, C18SFD-PUNIKKISO CO., LTD.K242176BLOOD TUBING LINES FOR HEMODIALYSIS AL Series (Archloop) BLOOD TUBING LINES FOR HEMODIALYSIS C18 Series (AL-ADC-E(U), AL-CDC-E(U), C18RDC-E(U), C18BDD-E(U), C18SFD-E(U)NIKKISO CO., LTD.K231589Blood Tubing Lines for Hemodialysis AV06C-ENIKKISO CO., LTD.K230514Blood Tubing Lines for Hemodialysis AL Series (Archloop), Blood Tubing Lines for Hemodialysis C18 SeriesNIKKISO CO., LTD.K201207CombiSet SMARTECH Hemodialysis Blood Tubing Set with attached Priming Set and Integrated Crit-Line Technology, CombiSet SMARTECH Hemodialysis Blood Tubing Set with attached Priming Set and Intergrated Crit-Line Technology, no Heparin LineFresenius Medical Care Renal Therapies Group, LLCK172238CAREline Airless Hemodialysis Blood Tubing SetsFresenius Medical Care Renal Therapies Group, LLC

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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