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FDA 510(k)

MULTIPLE ARTIFICIAL KIDNEY SYSTEMS (MAKS) #IDM

K-Number: K874084 · 1988-04-27

ApplicantNational Medical Care, Medical Products Div., Inc.
Decision Date1988-04-27
Product CodeFKQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MULTIPLE ARTIFICIAL KIDNEY SYSTEMS (MAKS) #IDM is the device name listed in this FDA 510(k) record. The listed applicant is National Medical Care, Medical Products Div., Inc.. It received FDA 510(k) clearance on 1988-04-27 under 510(k) number K874084. The device is classified under product code FKQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIPLE ARTIFICIAL KIDNEY SYSTEMS (MAKS) #IDM?

MULTIPLE ARTIFICIAL KIDNEY SYSTEMS (MAKS) #IDM is a medical device that received FDA 510(k) clearance on 1988-04-27. The listed applicant is National Medical Care, Medical Products Div., Inc.. The 510(k) number is K874084.

When did MULTIPLE ARTIFICIAL KIDNEY SYSTEMS (MAKS) #IDM receive FDA 510(k) clearance?

MULTIPLE ARTIFICIAL KIDNEY SYSTEMS (MAKS) #IDM received FDA 510(k) clearance on 1988-04-27, under 510(k) number K874084.

Who is the listed applicant for MULTIPLE ARTIFICIAL KIDNEY SYSTEMS (MAKS) #IDM?

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

What is the FDA product code for MULTIPLE ARTIFICIAL KIDNEY SYSTEMS (MAKS) #IDM?

The FDA product code for MULTIPLE ARTIFICIAL KIDNEY SYSTEMS (MAKS) #IDM is FKQ.

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Other records listing National Medical Care, Medical Products Div., 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.

K962081COMBILINES HEMODIALYSIS BLOOD TUBING SETK941757FORMALIN REUSE CARTK952343FOCUA 90R, 90HR, 120R, 120HR, 160R, 160HR HOLLOW FIBER DIALYZERK930843RAPID DISCONNECT Y-SET, CAT. NO. 48-7000K914790HOLLOW FIBER DIALYZER FOCUS 9OR/90H-R/120R/120H-RK920697DEXTROLYTE II PERITONEAL DIALYSIS 48-3029-7 CLAMP

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Related Devices (Code: FKQ)

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.

K052764DIACAP ULTRA DIALYSIS FLUID FILTERB. Braun Medizintechnologie GmbHK893612TWO TANK DISSOLUTION MODULENational Medical Care, Medical Products Div., Inc.K873421KAWASUMI A.V. FISTULA SETKawasumi Laboratories Co., Ltd.K870889ACID FUCHSIN SOLUTIONSD.R.G. Scientific IndustriesK861730ACTRIL FOR KIDNEY MACHINE DISINFECTANTRenal Systems, Inc.K864635FOUR TANK DISSOLUTION MODULENational Medical Care, Medical Products Div., 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.

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