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FDA 510(k)

AXIOM MULTIPURPOSE WOUND DRAIN

K-Number: K993592 · 2000-05-17

ApplicantAxiom Medical, Inc.
Decision Date2000-05-17
Product CodeBSO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AXIOM MULTIPURPOSE WOUND DRAIN 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 2000-05-17 under 510(k) number K993592. The device is classified under product code BSO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AXIOM MULTIPURPOSE WOUND DRAIN?

AXIOM MULTIPURPOSE WOUND DRAIN is a medical device that received FDA 510(k) clearance on 2000-05-17. The listed applicant is Axiom Medical, Inc.. The 510(k) number is K993592.

When did AXIOM MULTIPURPOSE WOUND DRAIN receive FDA 510(k) clearance?

AXIOM MULTIPURPOSE WOUND DRAIN received FDA 510(k) clearance on 2000-05-17, under 510(k) number K993592.

Who is the listed applicant for AXIOM MULTIPURPOSE WOUND DRAIN?

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 MULTIPURPOSE WOUND DRAIN?

The FDA product code for AXIOM MULTIPURPOSE WOUND DRAIN is BSO.

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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.

K971851INTERPLEURAL ANESTHESIA CATHETERK965146FLAT CLOSED WOUND DRAIN WITH TROCARK934895GLASSMAN SILICONE CATHETERK922760ATRAUM WOUND DRESSING--MODIFICATIONK905422PVC ROUND WOUND DRAINSK904218SUCTION SYSTEM

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Related Devices (Code: BSO)

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

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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