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FDA 510(k)

AXIOM FILTERED CONNECTOR

K-Number: K791508 · 1979-09-04

ApplicantAxiom Medical, Inc.
Decision Date1979-09-04
Product Code
DecisionSubstantially Equivalent

Device Summary

AXIOM FILTERED CONNECTOR 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 1979-09-04 under 510(k) number K791508. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AXIOM FILTERED CONNECTOR?

AXIOM FILTERED CONNECTOR is a medical device that received FDA 510(k) clearance on 1979-09-04. The listed applicant is Axiom Medical, Inc.. The 510(k) number is K791508.

When did AXIOM FILTERED CONNECTOR receive FDA 510(k) clearance?

AXIOM FILTERED CONNECTOR received FDA 510(k) clearance on 1979-09-04, under 510(k) number K791508.

Who is the listed applicant for AXIOM FILTERED CONNECTOR?

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

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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.

K993592AXIOM MULTIPURPOSE WOUND DRAINK971851INTERPLEURAL ANESTHESIA CATHETERK965146FLAT CLOSED WOUND DRAIN WITH TROCARK934895GLASSMAN SILICONE CATHETERK922760ATRAUM WOUND DRESSING--MODIFICATIONK905422PVC ROUND WOUND DRAINS

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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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