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FDA 510(k)

1BD SOLOSHOT IX SYRINGE

K-Number: K042934 · 2004-10-28

ApplicantBecton, Dickinson & CO
Decision Date2004-10-28
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

1BD SOLOSHOT IX SYRINGE 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 2004-10-28 under 510(k) number K042934. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 1BD SOLOSHOT IX SYRINGE?

1BD SOLOSHOT IX SYRINGE is a medical device that received FDA 510(k) clearance on 2004-10-28. The listed applicant is Becton, Dickinson & CO. The 510(k) number is K042934.

When did 1BD SOLOSHOT IX SYRINGE receive FDA 510(k) clearance?

1BD SOLOSHOT IX SYRINGE received FDA 510(k) clearance on 2004-10-28, under 510(k) number K042934.

Who is the listed applicant for 1BD SOLOSHOT IX SYRINGE?

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 1BD SOLOSHOT IX SYRINGE?

The FDA product code for 1BD SOLOSHOT IX SYRINGE is FMF.

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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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