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FDA 510(k)

SPRING GUIDE CATHETER ANESTHESIA CONDUCTION CATH

K-Number: K854601 · 1986-01-10

ApplicantConcord Laboratories, Inc.
Decision Date1986-01-10
Product CodeBSO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SPRING GUIDE CATHETER ANESTHESIA CONDUCTION CATH is the device name listed in this FDA 510(k) record. The listed applicant is Concord Laboratories, Inc.. It received FDA 510(k) clearance on 1986-01-10 under 510(k) number K854601. 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 SPRING GUIDE CATHETER ANESTHESIA CONDUCTION CATH?

SPRING GUIDE CATHETER ANESTHESIA CONDUCTION CATH is a medical device that received FDA 510(k) clearance on 1986-01-10. The listed applicant is Concord Laboratories, Inc.. The 510(k) number is K854601.

When did SPRING GUIDE CATHETER ANESTHESIA CONDUCTION CATH receive FDA 510(k) clearance?

SPRING GUIDE CATHETER ANESTHESIA CONDUCTION CATH received FDA 510(k) clearance on 1986-01-10, under 510(k) number K854601.

Who is the listed applicant for SPRING GUIDE CATHETER ANESTHESIA CONDUCTION CATH?

The FDA 510(k) record lists Concord Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPRING GUIDE CATHETER ANESTHESIA CONDUCTION CATH?

The FDA product code for SPRING GUIDE CATHETER ANESTHESIA CONDUCTION CATH is BSO.

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Other records listing Concord Laboratories, 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.

K883840DRI-VENT ARTERIAL BLOOD SAMPLING KITK871825MECONIUM SUCTION CATHETERK864535TRACHEOBRONCHIAL SUCTION CATHETER, CAT. NO. 6110K862039CONCORD CARE TRAYK854327SUBCUTANEOUS TUNNELING NEEDLES & HANDLESK851134REGIONAL ANESTHESIA TRAYS

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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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