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FDA 510(k)

MAR COR COMPLETE WATER TREATMENT SYSTEM FOR KDNEY DIALYSIS

K-Number: K945559 · 1996-05-28

Decision Date1996-05-28
Product CodeFIP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MAR COR COMPLETE WATER TREATMENT SYSTEM FOR KDNEY DIALYSIS is the device name listed in this FDA 510(k) record. The listed applicant is Mar Cor Services, Inc.. It received FDA 510(k) clearance on 1996-05-28 under 510(k) number K945559. 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 MAR COR COMPLETE WATER TREATMENT SYSTEM FOR KDNEY DIALYSIS?

MAR COR COMPLETE WATER TREATMENT SYSTEM FOR KDNEY DIALYSIS is a medical device that received FDA 510(k) clearance on 1996-05-28. The listed applicant is Mar Cor Services, Inc.. The 510(k) number is K945559.

When did MAR COR COMPLETE WATER TREATMENT SYSTEM FOR KDNEY DIALYSIS receive FDA 510(k) clearance?

MAR COR COMPLETE WATER TREATMENT SYSTEM FOR KDNEY DIALYSIS received FDA 510(k) clearance on 1996-05-28, under 510(k) number K945559.

Who is the listed applicant for MAR COR COMPLETE WATER TREATMENT SYSTEM FOR KDNEY DIALYSIS?

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

What is the FDA product code for MAR COR COMPLETE WATER TREATMENT SYSTEM FOR KDNEY DIALYSIS?

The FDA product code for MAR COR COMPLETE WATER TREATMENT SYSTEM FOR KDNEY DIALYSIS 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.

Other records listing Mar Cor Services, 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: 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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