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FDA 510(k)

SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260

K-Number: K831440 · 1983-06-03

ApplicantMed-West, Inc.
Decision Date1983-06-03
Product CodeFIQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260 is the device name listed in this FDA 510(k) record. The listed applicant is Med-West, Inc.. It received FDA 510(k) clearance on 1983-06-03 under 510(k) number K831440. The device is classified under product code FIQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260?

SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260 is a medical device that received FDA 510(k) clearance on 1983-06-03. The listed applicant is Med-West, Inc.. The 510(k) number is K831440.

When did SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260 receive FDA 510(k) clearance?

SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260 received FDA 510(k) clearance on 1983-06-03, under 510(k) number K831440.

Who is the listed applicant for SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260?

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

What is the FDA product code for SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260?

The FDA product code for SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260 is FIQ.

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Other records listing Med-West, Inc. as applicant

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Related Devices (Code: FIQ)

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.

K892887ST SERIES SAF-T-SHUNTS ARTERIOVENOUS CANNULAAkcess Medical Products, Inc.K892663S-100 ALLEN-BROWN SHUNTAkcess Medical Products, Inc.K892666SAF-T-SHUNT, S-300 SERIESAkcess Medical Products, Inc.K844692PEDIATRIC SIZED HEMOCATH CATHETERQuinton, Inc.K841791PLUME FISTULA NEEDLEHospal Medical Corp.K840322HEMOFILTRATION CATHETER HF-100Vas-Cath of Canada , Ltd.

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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