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FDA 510(k)

FIRST PICC CATHETER

K-Number: K972262 · 1997-09-15

ApplicantBecton Dickinson Infusion Therapy Systems, Inc.
Decision Date1997-09-15
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FIRST PICC CATHETER 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 K972262. 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?

FIRST PICC CATHETER 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 K972262.

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

FIRST PICC CATHETER received FDA 510(k) clearance on 1997-09-15, under 510(k) number K972262.

Who is the listed applicant for FIRST PICC CATHETER?

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?

The FDA product code for FIRST PICC CATHETER is FOZ.

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Other records listing Becton Dickinson Infusion Therapy Systems, Inc. as applicant

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Related Devices (Code: FOZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, Inc.

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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