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FDA 510(k)

DUAL SLIM PORT IMPLANTED PORT (0654970/0654940)

K-Number: K964066 · 1997-03-06

ApplicantC.R. Bard, Inc.
Decision Date1997-03-06
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DUAL SLIM PORT IMPLANTED PORT (0654970/0654940) 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 1997-03-06 under 510(k) number K964066. 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 DUAL SLIM PORT IMPLANTED PORT (0654970/0654940)?

DUAL SLIM PORT IMPLANTED PORT (0654970/0654940) is a medical device that received FDA 510(k) clearance on 1997-03-06. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K964066.

When did DUAL SLIM PORT IMPLANTED PORT (0654970/0654940) receive FDA 510(k) clearance?

DUAL SLIM PORT IMPLANTED PORT (0654970/0654940) received FDA 510(k) clearance on 1997-03-06, under 510(k) number K964066.

Who is the listed applicant for DUAL SLIM PORT IMPLANTED PORT (0654970/0654940)?

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 DUAL SLIM PORT IMPLANTED PORT (0654970/0654940)?

The FDA product code for DUAL SLIM PORT IMPLANTED PORT (0654970/0654940) 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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