FDA 510(k)

CORCATH H & B VASCULAR ACCESS CATHETER

K-Number: K823553 · 1983-01-05

ApplicantCormed, Inc., Sub. C.R.Bard, Inc.

Decision Date1983-01-05

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

CORCATH H & B VASCULAR ACCESS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Cormed, Inc., Sub. C.R.Bard, Inc.. It received FDA 510(k) clearance on 1983-01-05 under 510(k) number K823553. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORCATH H & B VASCULAR ACCESS CATHETER?

CORCATH H & B VASCULAR ACCESS CATHETER is a medical device that received FDA 510(k) clearance on 1983-01-05. The listed applicant is Cormed, Inc., Sub. C.R.Bard, Inc.. The 510(k) number is K823553.

When did CORCATH H & B VASCULAR ACCESS CATHETER receive FDA 510(k) clearance?

CORCATH H & B VASCULAR ACCESS CATHETER received FDA 510(k) clearance on 1983-01-05, under 510(k) number K823553.

Who is the listed applicant for CORCATH H & B VASCULAR ACCESS CATHETER?

The FDA 510(k) record lists Cormed, Inc., Sub. C.R.Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CORCATH H & B VASCULAR ACCESS CATHETER?

The FDA product code for CORCATH H & B VASCULAR ACCESS CATHETER is LJS.

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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.