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FDA 510(k)

BD VIPER INSTRUMENT

K-Number: K023955 · 2003-06-24

ApplicantBecton, Dickinson & CO
Decision Date2003-06-24
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BD VIPER INSTRUMENT 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 2003-06-24 under 510(k) number K023955. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD VIPER INSTRUMENT?

BD VIPER INSTRUMENT is a medical device that received FDA 510(k) clearance on 2003-06-24. The listed applicant is Becton, Dickinson & CO. The 510(k) number is K023955.

When did BD VIPER INSTRUMENT receive FDA 510(k) clearance?

BD VIPER INSTRUMENT received FDA 510(k) clearance on 2003-06-24, under 510(k) number K023955.

Who is the listed applicant for BD VIPER INSTRUMENT?

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 VIPER INSTRUMENT?

The FDA product code for BD VIPER INSTRUMENT is JQW.

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Related Devices (Code: JQW)

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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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