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FDA 510(k)

BBL CHROMAGAR 0157

K-Number: K070691 · 2007-11-20

ApplicantBecton, Dickinson & CO
Decision Date2007-11-20
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BBL CHROMAGAR 0157 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 2007-11-20 under 510(k) number K070691. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BBL CHROMAGAR 0157?

BBL CHROMAGAR 0157 is a medical device that received FDA 510(k) clearance on 2007-11-20. The listed applicant is Becton, Dickinson & CO. The 510(k) number is K070691.

When did BBL CHROMAGAR 0157 receive FDA 510(k) clearance?

BBL CHROMAGAR 0157 received FDA 510(k) clearance on 2007-11-20, under 510(k) number K070691.

Who is the listed applicant for BBL CHROMAGAR 0157?

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 BBL CHROMAGAR 0157?

The FDA product code for BBL CHROMAGAR 0157 is JSI.

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Related Devices (Code: JSI)

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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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