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FDA 510(k)

VASCULAR-ACCESS PORT CHANGE CATHETER

K-Number: K841150 · 1984-04-24

ApplicantNorfolk Medical Products, Inc.
Decision Date1984-04-24
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VASCULAR-ACCESS PORT CHANGE CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Norfolk Medical Products, Inc.. It received FDA 510(k) clearance on 1984-04-24 under 510(k) number K841150. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASCULAR-ACCESS PORT CHANGE CATHETER?

VASCULAR-ACCESS PORT CHANGE CATHETER is a medical device that received FDA 510(k) clearance on 1984-04-24. The listed applicant is Norfolk Medical Products, Inc.. The 510(k) number is K841150.

When did VASCULAR-ACCESS PORT CHANGE CATHETER receive FDA 510(k) clearance?

VASCULAR-ACCESS PORT CHANGE CATHETER received FDA 510(k) clearance on 1984-04-24, under 510(k) number K841150.

Who is the listed applicant for VASCULAR-ACCESS PORT CHANGE CATHETER?

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

What is the FDA product code for VASCULAR-ACCESS PORT CHANGE CATHETER?

The FDA product code for VASCULAR-ACCESS PORT CHANGE CATHETER is LJT.

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Other records listing Norfolk Medical Products, Inc. as applicant

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Related Devices (Code: LJT)

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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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