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FDA 510(k)

DISSCAP 110 DIALYZER

K-Number: K851380 · 1985-04-25

ApplicantHospal Medical Corp.
Decision Date1985-04-25
Product CodeFJI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DISSCAP 110 DIALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Hospal Medical Corp.. It received FDA 510(k) clearance on 1985-04-25 under 510(k) number K851380. 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 DISSCAP 110 DIALYZER?

DISSCAP 110 DIALYZER is a medical device that received FDA 510(k) clearance on 1985-04-25. The listed applicant is Hospal Medical Corp.. The 510(k) number is K851380.

When did DISSCAP 110 DIALYZER receive FDA 510(k) clearance?

DISSCAP 110 DIALYZER received FDA 510(k) clearance on 1985-04-25, under 510(k) number K851380.

Who is the listed applicant for DISSCAP 110 DIALYZER?

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

What is the FDA product code for DISSCAP 110 DIALYZER?

The FDA product code for DISSCAP 110 DIALYZER is FJI.

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Other records listing Hospal Medical Corp. 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.

K893742FILTRAL TM 20 HEMODIALYZER/FILTERK884365MULTIFLOW(TM) 60 KITK884326FILTRAL TM 8 HEMODIALYZERK883307CARDIOFLOW 100 HEMOCONCENTRATOR/PREPARATION KITK872767FILTRAL 10, FILTRAL 12, FILTRAL 16 HEMODIALYZERK871218MONITRAL S GS HEMODIALYSIS SINGLE PATIENT UNIT

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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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