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FDA 510(k)

INTERPLEURAL ANESTHESIA CATHETER

K-Number: K971851 · 1998-01-22

ApplicantAxiom Medical, Inc.
Decision Date1998-01-22
Product CodeBSO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INTERPLEURAL ANESTHESIA 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 1998-01-22 under 510(k) number K971851. 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 INTERPLEURAL ANESTHESIA CATHETER?

INTERPLEURAL ANESTHESIA CATHETER is a medical device that received FDA 510(k) clearance on 1998-01-22. The listed applicant is Axiom Medical, Inc.. The 510(k) number is K971851.

When did INTERPLEURAL ANESTHESIA CATHETER receive FDA 510(k) clearance?

INTERPLEURAL ANESTHESIA CATHETER received FDA 510(k) clearance on 1998-01-22, under 510(k) number K971851.

Who is the listed applicant for INTERPLEURAL ANESTHESIA 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 INTERPLEURAL ANESTHESIA CATHETER?

The FDA product code for INTERPLEURAL ANESTHESIA CATHETER 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.

K993592AXIOM MULTIPURPOSE WOUND DRAINK965146FLAT 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.

K241410EDEN ControlCathJmt Co., Ltd.K231242Perifix FX Catheter; Contiplex FX CatheterB.Braun Medical, Inc.K230603Arrow Non-Stimulating SnapLock Adapter (K-05520-005C); Arrow Non-Stimulating Next Gen SnapLock Adapter (Luer Connection) (CA-000010-19); Arrow Non-Stimulating Next Gen SnapLock Adapter (Neuraxial Connection) (CA-000014-19); Arrow Stimulating SnapLock Adapter (with cable) (TZ-02060-001); Arrow Stimulating SnapLock Adapter (with tab) (TZ-05000-002)Teleflex MedicalK193664SubQKath Catheter and Needle SetHk SurgicalK200624Percutaneous IntroducerEpimed International, Inc.K191470C-CAT Anaesthesia Catheter kitCimpax Aps

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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