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FDA 510(k)

DIALYZER, PARALLEL FLOW DISPOSABLE

K-Number: K781795 · 1978-12-15

ApplicantMedical, Inc.
Decision Date1978-12-15
Product CodeFJG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DIALYZER, PARALLEL FLOW DISPOSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Medical, Inc.. It received FDA 510(k) clearance on 1978-12-15 under 510(k) number K781795. The device is classified under product code FJG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIALYZER, PARALLEL FLOW DISPOSABLE?

DIALYZER, PARALLEL FLOW DISPOSABLE is a medical device that received FDA 510(k) clearance on 1978-12-15. The listed applicant is Medical, Inc.. The 510(k) number is K781795.

When did DIALYZER, PARALLEL FLOW DISPOSABLE receive FDA 510(k) clearance?

DIALYZER, PARALLEL FLOW DISPOSABLE received FDA 510(k) clearance on 1978-12-15, under 510(k) number K781795.

Who is the listed applicant for DIALYZER, PARALLEL FLOW DISPOSABLE?

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

What is the FDA product code for DIALYZER, PARALLEL FLOW DISPOSABLE?

The FDA product code for DIALYZER, PARALLEL FLOW DISPOSABLE is FJG.

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Other records listing Medical, 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.

K926454ANESTHESIA RESPIRATORY BREATH CIRCUIT PACKS/COMPONK894839OS-1 OCCLUSION SYSTEM - 1K872001MODEL TPC-1A OXYGEN ANALYZERK863806MODEL A-1 OXYGEN ANALYZERK862609INTERFACE ARTERIAL BLOOD FILTER, MODEL 44K862591INTERFACE ARTERIAL BLOOD FILTER, MODEL 42

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Related Devices (Code: FJG)

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.

K933681GAMBRO LUNDIA PRO 100, 500, 600 DIALYZERSCobe Renal Care, Inc.K933680GAMBRO LUNDIA PRO 200 DIALYZERCobe Renal Care, Inc.K920693DEXTROLYTE II PERITONEAL DIALYSIS 48-3028-9National Medical Care, Medical Products Div., Inc.K915504GAMBRO LUNDIA ALPHA HEMODIALYZERSC.G.H. Medical, Inc.K901368HEMOSPAL KITS A1, A2D, AO, & A1DGambro-Hospal, Inc.K902203TENCKHOFF PERITONEAL DIALYSIS KITAkcess Medical Products, 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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