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FDA 510(k)

BD VIPER SYSTEM

K-Number: K052481 · 2005-11-28

ApplicantBecton, Dickinson & CO
Decision Date2005-11-28
Product CodeLSL
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BD VIPER SYSTEM 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 2005-11-28 under 510(k) number K052481. The device is classified under product code LSL. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD VIPER SYSTEM?

BD VIPER SYSTEM is a medical device that received FDA 510(k) clearance on 2005-11-28. The listed applicant is Becton, Dickinson & CO. The 510(k) number is K052481.

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

BD VIPER SYSTEM received FDA 510(k) clearance on 2005-11-28, under 510(k) number K052481.

Who is the listed applicant for BD VIPER SYSTEM?

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 SYSTEM?

The FDA product code for BD VIPER SYSTEM is LSL.

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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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