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FDA 510(k)

EVANS, VAS-CATH EPIDURAL NEEDLE & CATHETER

K-Number: K850009 · 1985-05-13

ApplicantVas-Cath of Canada , Ltd.
Decision Date1985-05-13
Product CodeBSO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EVANS, VAS-CATH EPIDURAL NEEDLE & CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Vas-Cath of Canada , Ltd.. It received FDA 510(k) clearance on 1985-05-13 under 510(k) number K850009. 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 EVANS, VAS-CATH EPIDURAL NEEDLE & CATHETER?

EVANS, VAS-CATH EPIDURAL NEEDLE & CATHETER is a medical device that received FDA 510(k) clearance on 1985-05-13. The listed applicant is Vas-Cath of Canada , Ltd.. The 510(k) number is K850009.

When did EVANS, VAS-CATH EPIDURAL NEEDLE & CATHETER receive FDA 510(k) clearance?

EVANS, VAS-CATH EPIDURAL NEEDLE & CATHETER received FDA 510(k) clearance on 1985-05-13, under 510(k) number K850009.

Who is the listed applicant for EVANS, VAS-CATH EPIDURAL NEEDLE & CATHETER?

The FDA 510(k) record lists Vas-Cath of Canada , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EVANS, VAS-CATH EPIDURAL NEEDLE & CATHETER?

The FDA product code for EVANS, VAS-CATH EPIDURAL NEEDLE & CATHETER is BSO.

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.

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Other records listing Vas-Cath of Canada , Ltd. 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.

K875188LUER LOCK CONNECTORS / RIDIG P.V.C.K871817VAS-CATH PERITONEAL DIALYSIS CATHETERK871487VAS-CATH PERMANENT SINGLE LUMEN HEMODIALYSIS CATHK871488VAS-CATH PERMANENT DUAL LUMEN HEMODIALYSIS CATHK863982VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAYK853283VACCESS TM 4006

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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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