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FDA 510(k)

HICKMAN SUBCUTANEOUS PORT W/PRE-ATTACHED CATHETER

K-Number: K863305 · 1986-10-10

ApplicantC.R. Bard, Inc.
Decision Date1986-10-10
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HICKMAN SUBCUTANEOUS PORT W/PRE-ATTACHED CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1986-10-10 under 510(k) number K863305. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HICKMAN SUBCUTANEOUS PORT W/PRE-ATTACHED CATHETER?

HICKMAN SUBCUTANEOUS PORT W/PRE-ATTACHED CATHETER is a medical device that received FDA 510(k) clearance on 1986-10-10. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K863305.

When did HICKMAN SUBCUTANEOUS PORT W/PRE-ATTACHED CATHETER receive FDA 510(k) clearance?

HICKMAN SUBCUTANEOUS PORT W/PRE-ATTACHED CATHETER received FDA 510(k) clearance on 1986-10-10, under 510(k) number K863305.

Who is the listed applicant for HICKMAN SUBCUTANEOUS PORT W/PRE-ATTACHED CATHETER?

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

What is the FDA product code for HICKMAN SUBCUTANEOUS PORT W/PRE-ATTACHED CATHETER?

The FDA product code for HICKMAN SUBCUTANEOUS PORT W/PRE-ATTACHED CATHETER is LJT.

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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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