FDA 510(k)

QMS LIDOCAINE CALIBRATORS, MODEL 0374678

K-Number: K091617 · 2009-07-17

Decision Date2009-07-17

Product CodeDLJ

Advisory CommitteeTX

DecisionSubstantially Equivalent

Device Summary

QMS LIDOCAINE CALIBRATORS, MODEL 0374678 is the device name listed in this FDA 510(k) record. The listed applicant is Thermo Fisher Scientific. It received FDA 510(k) clearance on 2009-07-17 under 510(k) number K091617. The device is classified under product code DLJ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QMS LIDOCAINE CALIBRATORS, MODEL 0374678?

QMS LIDOCAINE CALIBRATORS, MODEL 0374678 is a medical device that received FDA 510(k) clearance on 2009-07-17. The listed applicant is Thermo Fisher Scientific. The 510(k) number is K091617.

When did QMS LIDOCAINE CALIBRATORS, MODEL 0374678 receive FDA 510(k) clearance?

QMS LIDOCAINE CALIBRATORS, MODEL 0374678 received FDA 510(k) clearance on 2009-07-17, under 510(k) number K091617.

Who is the listed applicant for QMS LIDOCAINE CALIBRATORS, MODEL 0374678?

The FDA 510(k) record lists Thermo Fisher Scientific as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QMS LIDOCAINE CALIBRATORS, MODEL 0374678?

The FDA product code for QMS LIDOCAINE CALIBRATORS, MODEL 0374678 is DLJ.

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Related Devices (Code: DLJ)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.