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FDA 510(k)

DIALYZER STANDARD, CODE 5DM1780

K-Number: K772318 · 1978-01-26

Decision Date1978-01-26
Product CodeFJG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DIALYZER STANDARD, CODE 5DM1780 is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1978-01-26 under 510(k) number K772318. 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 STANDARD, CODE 5DM1780?

DIALYZER STANDARD, CODE 5DM1780 is a medical device that received FDA 510(k) clearance on 1978-01-26. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K772318.

When did DIALYZER STANDARD, CODE 5DM1780 receive FDA 510(k) clearance?

DIALYZER STANDARD, CODE 5DM1780 received FDA 510(k) clearance on 1978-01-26, under 510(k) number K772318.

Who is the listed applicant for DIALYZER STANDARD, CODE 5DM1780?

The FDA 510(k) record lists Travenol Laboratories, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIALYZER STANDARD, CODE 5DM1780?

The FDA product code for DIALYZER STANDARD, CODE 5DM1780 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 Travenol Laboratories, S.A. 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.

View all 206 devices →

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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