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FDA 510(k)

CENTRAL VEIN CATHETERIZATION TRAY

K-Number: K852642 · 1986-01-16

ApplicantTeleflexmedical, Inc.
Decision Date1986-01-16
Product CodeFDZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CENTRAL VEIN CATHETERIZATION TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Teleflexmedical, Inc.. It received FDA 510(k) clearance on 1986-01-16 under 510(k) number K852642. The device is classified under product code FDZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRAL VEIN CATHETERIZATION TRAY?

CENTRAL VEIN CATHETERIZATION TRAY is a medical device that received FDA 510(k) clearance on 1986-01-16. The listed applicant is Teleflexmedical, Inc.. The 510(k) number is K852642.

When did CENTRAL VEIN CATHETERIZATION TRAY receive FDA 510(k) clearance?

CENTRAL VEIN CATHETERIZATION TRAY received FDA 510(k) clearance on 1986-01-16, under 510(k) number K852642.

Who is the listed applicant for CENTRAL VEIN CATHETERIZATION TRAY?

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

What is the FDA product code for CENTRAL VEIN CATHETERIZATION TRAY?

The FDA product code for CENTRAL VEIN CATHETERIZATION TRAY is FDZ.

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Related Devices (Code: FDZ)

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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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