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FDA 510(k)

EPINEED EPIDURAL CATHETER

K-Number: K832232 · 1983-08-08

ApplicantTerumo Medical Corp.
Decision Date1983-08-08
Product CodeBSO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EPINEED EPIDURAL CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Medical Corp.. It received FDA 510(k) clearance on 1983-08-08 under 510(k) number K832232. 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 EPINEED EPIDURAL CATHETER?

EPINEED EPIDURAL CATHETER is a medical device that received FDA 510(k) clearance on 1983-08-08. The listed applicant is Terumo Medical Corp.. The 510(k) number is K832232.

When did EPINEED EPIDURAL CATHETER receive FDA 510(k) clearance?

EPINEED EPIDURAL CATHETER received FDA 510(k) clearance on 1983-08-08, under 510(k) number K832232.

Who is the listed applicant for EPINEED EPIDURAL CATHETER?

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

What is the FDA product code for EPINEED EPIDURAL CATHETER?

The FDA product code for EPINEED EPIDURAL CATHETER is BSO.

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Other records listing Terumo Medical Corp. 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.

K111606PINNACLE PRECISION ACCESS SYSTEMK111556GLIDECROSS SUPPORT CATHETERK110540TERUMO SUPPORT CATHETERK102008GLIDESHEATHK091329PINNACLE DESTINATION PERIPHERAL GUIDING SHEATHK082997TERUMO HYBRIA CLOSED SYSTEM SAFETY I.V. CATHETER

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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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