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FDA 510(k)

CENTRAL VENOUS CATHETER, DRESSING CHANGE KIT, STER

K-Number: K920846 · 1992-09-01

ApplicantTrinity Laboratories, Inc.
Decision Date1992-09-01
Product CodeFXX
Advisory CommitteeSU
DecisionUnknown

Device Summary

CENTRAL VENOUS CATHETER, DRESSING CHANGE KIT, STER is the device name listed in this FDA 510(k) record. The listed applicant is Trinity Laboratories, Inc.. It received FDA 510(k) clearance on 1992-09-01 under 510(k) number K920846. The device is classified under product code FXX. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CENTRAL VENOUS CATHETER, DRESSING CHANGE KIT, STER?

CENTRAL VENOUS CATHETER, DRESSING CHANGE KIT, STER is a medical device that received FDA 510(k) clearance on 1992-09-01. The listed applicant is Trinity Laboratories, Inc.. The 510(k) number is K920846.

When did CENTRAL VENOUS CATHETER, DRESSING CHANGE KIT, STER receive FDA 510(k) clearance?

CENTRAL VENOUS CATHETER, DRESSING CHANGE KIT, STER received FDA 510(k) clearance on 1992-09-01, under 510(k) number K920846.

Who is the listed applicant for CENTRAL VENOUS CATHETER, DRESSING CHANGE KIT, STER?

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

What is the FDA product code for CENTRAL VENOUS CATHETER, DRESSING CHANGE KIT, STER?

The FDA product code for CENTRAL VENOUS CATHETER, DRESSING CHANGE KIT, STER is FXX.

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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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