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FDA 510(k)

BD VACUTAINER PLUS PLASTIC URINE C&S PRESERVAYIVE TUBES AND KITS

K-Number: K024240 · 2003-03-26

ApplicantBd
Decision Date2003-03-26
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BD VACUTAINER PLUS PLASTIC URINE C&S PRESERVAYIVE TUBES AND KITS is the device name listed in this FDA 510(k) record. The listed applicant is Bd. It received FDA 510(k) clearance on 2003-03-26 under 510(k) number K024240. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD VACUTAINER PLUS PLASTIC URINE C&S PRESERVAYIVE TUBES AND KITS?

BD VACUTAINER PLUS PLASTIC URINE C&S PRESERVAYIVE TUBES AND KITS is a medical device that received FDA 510(k) clearance on 2003-03-26. The listed applicant is Bd. The 510(k) number is K024240.

When did BD VACUTAINER PLUS PLASTIC URINE C&S PRESERVAYIVE TUBES AND KITS receive FDA 510(k) clearance?

BD VACUTAINER PLUS PLASTIC URINE C&S PRESERVAYIVE TUBES AND KITS received FDA 510(k) clearance on 2003-03-26, under 510(k) number K024240.

Who is the listed applicant for BD VACUTAINER PLUS PLASTIC URINE C&S PRESERVAYIVE TUBES AND KITS?

The FDA 510(k) record lists Bd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD VACUTAINER PLUS PLASTIC URINE C&S PRESERVAYIVE TUBES AND KITS?

The FDA product code for BD VACUTAINER PLUS PLASTIC URINE C&S PRESERVAYIVE TUBES AND KITS is JSM.

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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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