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FDA 510(k)

AXIOM THORACIC CATHETERS

K-Number: K841593 · 1984-06-05

Decision Date1984-06-05
Product Code
DecisionSubstantially Equivalent

Device Summary

AXIOM THORACIC CATHETERS 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 1984-06-05 under 510(k) number K841593. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AXIOM THORACIC CATHETERS?

AXIOM THORACIC CATHETERS is a medical device that received FDA 510(k) clearance on 1984-06-05. The listed applicant is Axiom Medical, Inc.. The 510(k) number is K841593.

When did AXIOM THORACIC CATHETERS receive FDA 510(k) clearance?

AXIOM THORACIC CATHETERS received FDA 510(k) clearance on 1984-06-05, under 510(k) number K841593.

Who is the listed applicant for AXIOM THORACIC CATHETERS?

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

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 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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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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