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FDA 510(k)

CENTRAL CATHETER TRAY

K-Number: K781333 · 1978-10-24

ApplicantArgon Medical Corp.
Decision Date1978-10-24
Product CodeKGC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CENTRAL CATHETER TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Argon Medical Corp.. It received FDA 510(k) clearance on 1978-10-24 under 510(k) number K781333. The device is classified under product code KGC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRAL CATHETER TRAY?

CENTRAL CATHETER TRAY is a medical device that received FDA 510(k) clearance on 1978-10-24. The listed applicant is Argon Medical Corp.. The 510(k) number is K781333.

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

CENTRAL CATHETER TRAY received FDA 510(k) clearance on 1978-10-24, under 510(k) number K781333.

Who is the listed applicant for CENTRAL CATHETER TRAY?

The FDA 510(k) record lists Argon Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CENTRAL CATHETER TRAY?

The FDA product code for CENTRAL CATHETER TRAY is KGC.

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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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