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FDA 510(k)

ARTEOIAL BLOOD SAMPLING KIT 2D9014

K-Number: K771584 · 1977-09-13

ApplicantTravenol Laboratories, S.A.
Decision Date1977-09-13
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ARTEOIAL BLOOD SAMPLING KIT 2D9014 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 1977-09-13 under 510(k) number K771584. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTEOIAL BLOOD SAMPLING KIT 2D9014?

ARTEOIAL BLOOD SAMPLING KIT 2D9014 is a medical device that received FDA 510(k) clearance on 1977-09-13. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K771584.

When did ARTEOIAL BLOOD SAMPLING KIT 2D9014 receive FDA 510(k) clearance?

ARTEOIAL BLOOD SAMPLING KIT 2D9014 received FDA 510(k) clearance on 1977-09-13, under 510(k) number K771584.

Who is the listed applicant for ARTEOIAL BLOOD SAMPLING KIT 2D9014?

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 ARTEOIAL BLOOD SAMPLING KIT 2D9014?

The FDA product code for ARTEOIAL BLOOD SAMPLING KIT 2D9014 is FMF.

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Other records listing Travenol Laboratories, S.A. as applicant

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Related Devices (Code: FMF)

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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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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