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FDA 510(k)

FIRST PICC INTRODUCER CATHETER

K-Number: K954906 · 1996-04-08

Decision Date1996-04-08
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FIRST PICC INTRODUCER CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Vascular Access, Inc.. It received FDA 510(k) clearance on 1996-04-08 under 510(k) number K954906. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIRST PICC INTRODUCER CATHETER?

FIRST PICC INTRODUCER CATHETER is a medical device that received FDA 510(k) clearance on 1996-04-08. The listed applicant is Becton Dickinson Vascular Access, Inc.. The 510(k) number is K954906.

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

FIRST PICC INTRODUCER CATHETER received FDA 510(k) clearance on 1996-04-08, under 510(k) number K954906.

Who is the listed applicant for FIRST PICC INTRODUCER CATHETER?

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

What is the FDA product code for FIRST PICC INTRODUCER CATHETER?

The FDA product code for FIRST PICC INTRODUCER CATHETER is DYB.

Related Clinical Trials

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.

Other records listing Becton Dickinson Vascular Access, Inc. as applicant

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.

View all 25 devices →

Related Devices (Code: DYB)

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.

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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