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FDA 510(k)

GAMBRO LUNDIA PLATE DIALYZER

K-Number: K792611 · 1980-02-06

ApplicantGambro, Inc.
Decision Date1980-02-06
Product CodeFJG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GAMBRO LUNDIA PLATE DIALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Gambro, Inc.. It received FDA 510(k) clearance on 1980-02-06 under 510(k) number K792611. 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 GAMBRO LUNDIA PLATE DIALYZER?

GAMBRO LUNDIA PLATE DIALYZER is a medical device that received FDA 510(k) clearance on 1980-02-06. The listed applicant is Gambro, Inc.. The 510(k) number is K792611.

When did GAMBRO LUNDIA PLATE DIALYZER receive FDA 510(k) clearance?

GAMBRO LUNDIA PLATE DIALYZER received FDA 510(k) clearance on 1980-02-06, under 510(k) number K792611.

Who is the listed applicant for GAMBRO LUNDIA PLATE DIALYZER?

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 GAMBRO LUNDIA PLATE DIALYZER?

The FDA product code for GAMBRO LUNDIA PLATE DIALYZER is FJG.

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 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.

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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.

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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