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FDA 510(k)

GF 120M, 120H, 180M & 180H HOLLOW FIBER DIALYZERS

K-Number: K880084 · 1988-02-19

ApplicantGambro, Inc.
Decision Date1988-02-19
Product CodeFJI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GF 120M, 120H, 180M & 180H HOLLOW FIBER DIALYZERS is the device name listed in this FDA 510(k) record. The listed applicant is Gambro, Inc.. It received FDA 510(k) clearance on 1988-02-19 under 510(k) number K880084. The device is classified under product code FJI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GF 120M, 120H, 180M & 180H HOLLOW FIBER DIALYZERS?

GF 120M, 120H, 180M & 180H HOLLOW FIBER DIALYZERS is a medical device that received FDA 510(k) clearance on 1988-02-19. The listed applicant is Gambro, Inc.. The 510(k) number is K880084.

When did GF 120M, 120H, 180M & 180H HOLLOW FIBER DIALYZERS receive FDA 510(k) clearance?

GF 120M, 120H, 180M & 180H HOLLOW FIBER DIALYZERS received FDA 510(k) clearance on 1988-02-19, under 510(k) number K880084.

Who is the listed applicant for GF 120M, 120H, 180M & 180H HOLLOW FIBER DIALYZERS?

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

What is the FDA product code for GF 120M, 120H, 180M & 180H HOLLOW FIBER DIALYZERS?

The FDA product code for GF 120M, 120H, 180M & 180H HOLLOW FIBER DIALYZERS is FJI.

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Other records listing Gambro, 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.

K083158EXALIS, SOFTWARE VERSION 1.15K070643PHOENIX HEMODIALYSIS DELIVERY SYSTEM, VERSION 3.35K032431PRISMA M60/M100 SETSK896758GAMBRO BICARBONATE MONITOR BCM 10-3K896757GAMBRO AK-10 DIALYSIS SYSTEM FOR HIGH FLOWSK902481GAMBRO ALWALL GFS PLUS 11, 16 & 20 HOLLOW FIBER

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Related Devices (Code: FJI)

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.

K190459Hemoflow F3 and F4 DialyzersFresenius Medical Care Renal Therapies Group, LLCK122952NIPRO PUREFLUX-L HEMODIALYZERNipro Medical CorporationK043342POLYFLUX FAMILY HEMODIALYZER/FILTER LABELED FOR SINGLE AND MULTIPLE USE, MODELS 14L, 17L, 21L, 140H, 170H, 210H,6LR, 8LRGambro Renal ProductsK010366DISPOSABLE STORAGE CAPMolded Products, Inc.K011148ULTRACONCENTRATOR SYSTEMInterpore Cross Intl.K002761FRESNIUS HEMOFLOW F7NR, F50NR, F70NR HEMODIALYZERSFresenius Medical Care North America

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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