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FDA 510(k)

FILTER FOR HYPERALIMENTATION SET

K-Number: K782134 · 1979-01-17

Decision Date1979-01-17
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FILTER FOR HYPERALIMENTATION SET 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 1979-01-17 under 510(k) number K782134. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FILTER FOR HYPERALIMENTATION SET?

FILTER FOR HYPERALIMENTATION SET is a medical device that received FDA 510(k) clearance on 1979-01-17. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K782134.

When did FILTER FOR HYPERALIMENTATION SET receive FDA 510(k) clearance?

FILTER FOR HYPERALIMENTATION SET received FDA 510(k) clearance on 1979-01-17, under 510(k) number K782134.

Who is the listed applicant for FILTER FOR HYPERALIMENTATION SET?

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 FILTER FOR HYPERALIMENTATION SET?

The FDA product code for FILTER FOR HYPERALIMENTATION SET is FPA.

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: FPA)

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

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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