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FDA 510(k)

HICKMAN TITANIUM SUBCUTANEOUS PORT

K-Number: K870260 · 1987-04-15

ApplicantC.R. Bard, Inc.
Decision Date1987-04-15
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HICKMAN TITANIUM SUBCUTANEOUS PORT 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 1987-04-15 under 510(k) number K870260. 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 TITANIUM SUBCUTANEOUS PORT?

HICKMAN TITANIUM SUBCUTANEOUS PORT is a medical device that received FDA 510(k) clearance on 1987-04-15. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K870260.

When did HICKMAN TITANIUM SUBCUTANEOUS PORT receive FDA 510(k) clearance?

HICKMAN TITANIUM SUBCUTANEOUS PORT received FDA 510(k) clearance on 1987-04-15, under 510(k) number K870260.

Who is the listed applicant for HICKMAN TITANIUM SUBCUTANEOUS PORT?

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 TITANIUM SUBCUTANEOUS PORT?

The FDA product code for HICKMAN TITANIUM SUBCUTANEOUS PORT is LJT.

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Related Devices (Code: 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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