FDA 510(k)

CENTRAL VEIN CATH. TRAY CC-20-1420

K-Number: K833573 · 1984-01-11

Decision Date1984-01-11

Product CodeDQY

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CENTRAL VEIN CATH. TRAY CC-20-1420 is the device name listed in this FDA 510(k) record. The listed applicant is Intermed, Inc.. It received FDA 510(k) clearance on 1984-01-11 under 510(k) number K833573. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRAL VEIN CATH. TRAY CC-20-1420?

CENTRAL VEIN CATH. TRAY CC-20-1420 is a medical device that received FDA 510(k) clearance on 1984-01-11. The listed applicant is Intermed, Inc.. The 510(k) number is K833573.

When did CENTRAL VEIN CATH. TRAY CC-20-1420 receive FDA 510(k) clearance?

CENTRAL VEIN CATH. TRAY CC-20-1420 received FDA 510(k) clearance on 1984-01-11, under 510(k) number K833573.

Who is the listed applicant for CENTRAL VEIN CATH. TRAY CC-20-1420?

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

What is the FDA product code for CENTRAL VEIN CATH. TRAY CC-20-1420?

The FDA product code for CENTRAL VEIN CATH. TRAY CC-20-1420 is DQY.

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Other records listing Intermed, Inc. as applicant

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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.