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FDA 510(k)

BD VACUTAINER SAFETY-LOK ADMINISTRATION SET WITH FILTER

K-Number: K033350 · 2003-11-18

Decision Date2003-11-18
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BD VACUTAINER SAFETY-LOK ADMINISTRATION SET WITH FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson & CO. It received FDA 510(k) clearance on 2003-11-18 under 510(k) number K033350. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD VACUTAINER SAFETY-LOK ADMINISTRATION SET WITH FILTER?

BD VACUTAINER SAFETY-LOK ADMINISTRATION SET WITH FILTER is a medical device that received FDA 510(k) clearance on 2003-11-18. The listed applicant is Becton, Dickinson & CO. The 510(k) number is K033350.

When did BD VACUTAINER SAFETY-LOK ADMINISTRATION SET WITH FILTER receive FDA 510(k) clearance?

BD VACUTAINER SAFETY-LOK ADMINISTRATION SET WITH FILTER received FDA 510(k) clearance on 2003-11-18, under 510(k) number K033350.

Who is the listed applicant for BD VACUTAINER SAFETY-LOK ADMINISTRATION SET WITH FILTER?

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

What is the FDA product code for BD VACUTAINER SAFETY-LOK ADMINISTRATION SET WITH FILTER?

The FDA product code for BD VACUTAINER SAFETY-LOK ADMINISTRATION SET WITH FILTER is FPA.

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 & CO 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 190 devices →

Related Devices (Code: FPA)

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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