FDA 510(k)

VASCULAR ACCESS PORT CHANGES IN MATER

K-Number: K840788 · 1984-04-24

Decision Date1984-04-24

Product CodeLJT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

VASCULAR ACCESS PORT CHANGES IN MATER 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 K840788. 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 CHANGES IN MATER?

VASCULAR ACCESS PORT CHANGES IN MATER 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 K840788.

When did VASCULAR ACCESS PORT CHANGES IN MATER receive FDA 510(k) clearance?

VASCULAR ACCESS PORT CHANGES IN MATER received FDA 510(k) clearance on 1984-04-24, under 510(k) number K840788.

Who is the listed applicant for VASCULAR ACCESS PORT CHANGES IN MATER?

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 CHANGES IN MATER?

The FDA product code for VASCULAR ACCESS PORT CHANGES IN MATER 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.