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FDA 510(k)

CATHETER THORACIC, AXIOM

K-Number: K770983 · 1977-07-29

ApplicantAxiom Medical, Inc.
Decision Date1977-07-29
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CATHETER THORACIC, AXIOM 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 1977-07-29 under 510(k) number K770983. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER THORACIC, AXIOM?

CATHETER THORACIC, AXIOM is a medical device that received FDA 510(k) clearance on 1977-07-29. The listed applicant is Axiom Medical, Inc.. The 510(k) number is K770983.

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

CATHETER THORACIC, AXIOM received FDA 510(k) clearance on 1977-07-29, under 510(k) number K770983.

Who is the listed applicant for CATHETER THORACIC, AXIOM?

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 CATHETER THORACIC, AXIOM?

The FDA product code for CATHETER THORACIC, AXIOM is JOL.

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Other records listing Axiom Medical, Inc. as applicant

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Related Devices (Code: JOL)

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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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