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FDA 510(k)

TELAVANCIN 30 UG, BBL SENSI-DISC

K-Number: K100722 · 2010-03-29

ApplicantBecton, Dickinson and Company
Decision Date2010-03-29
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TELAVANCIN 30 UG, BBL SENSI-DISC is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson and Company. It received FDA 510(k) clearance on 2010-03-29 under 510(k) number K100722. The device is classified under product code JTN. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TELAVANCIN 30 UG, BBL SENSI-DISC?

TELAVANCIN 30 UG, BBL SENSI-DISC is a medical device that received FDA 510(k) clearance on 2010-03-29. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K100722.

When did TELAVANCIN 30 UG, BBL SENSI-DISC receive FDA 510(k) clearance?

TELAVANCIN 30 UG, BBL SENSI-DISC received FDA 510(k) clearance on 2010-03-29, under 510(k) number K100722.

Who is the listed applicant for TELAVANCIN 30 UG, BBL SENSI-DISC?

The FDA 510(k) record lists Becton, Dickinson and Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TELAVANCIN 30 UG, BBL SENSI-DISC?

The FDA product code for TELAVANCIN 30 UG, BBL SENSI-DISC is JTN.

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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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