FDA 510(k)

FIRST PICC CATHETER WITH DUAL LUMENS

K-Number: K972263 · 1997-09-15

ApplicantBecton Dickinson Infusion Therapy Systems, Inc.

Decision Date1997-09-15

Product CodeFOZ

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

FIRST PICC CATHETER WITH DUAL LUMENS is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Infusion Therapy Systems, Inc.. It received FDA 510(k) clearance on 1997-09-15 under 510(k) number K972263. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIRST PICC CATHETER WITH DUAL LUMENS?

FIRST PICC CATHETER WITH DUAL LUMENS is a medical device that received FDA 510(k) clearance on 1997-09-15. The listed applicant is Becton Dickinson Infusion Therapy Systems, Inc.. The 510(k) number is K972263.

When did FIRST PICC CATHETER WITH DUAL LUMENS receive FDA 510(k) clearance?

FIRST PICC CATHETER WITH DUAL LUMENS received FDA 510(k) clearance on 1997-09-15, under 510(k) number K972263.

Who is the listed applicant for FIRST PICC CATHETER WITH DUAL LUMENS?

The FDA 510(k) record lists Becton Dickinson Infusion Therapy Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FIRST PICC CATHETER WITH DUAL LUMENS?

The FDA product code for FIRST PICC CATHETER WITH DUAL LUMENS is FOZ.

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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.