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FDA 510(k)

AXIOM FEMORAL VENUS CATHETER

K-Number: K842084 · 1984-08-01

ApplicantAxiom Medical, Inc.
Decision Date1984-08-01
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AXIOM FEMORAL VENUS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Axiom Medical, Inc.. It received FDA 510(k) clearance on 1984-08-01 under 510(k) number K842084. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AXIOM FEMORAL VENUS CATHETER?

AXIOM FEMORAL VENUS CATHETER is a medical device that received FDA 510(k) clearance on 1984-08-01. The listed applicant is Axiom Medical, Inc.. The 510(k) number is K842084.

When did AXIOM FEMORAL VENUS CATHETER receive FDA 510(k) clearance?

AXIOM FEMORAL VENUS CATHETER received FDA 510(k) clearance on 1984-08-01, under 510(k) number K842084.

Who is the listed applicant for AXIOM FEMORAL VENUS CATHETER?

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

What is the FDA product code for AXIOM FEMORAL VENUS CATHETER?

The FDA product code for AXIOM FEMORAL VENUS CATHETER is DQY.

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Other records listing Axiom 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.

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Related Devices (Code: DQY)

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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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