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FDA 510(k)

LIEBEL-FLARSHEIM DIRECT DIGITAL IMAGING SYSTEM

K-Number: K121838 · 2012-07-11

ApplicantLiebel-Flarsheim
Decision Date2012-07-11
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LIEBEL-FLARSHEIM DIRECT DIGITAL IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Liebel-Flarsheim. It received FDA 510(k) clearance on 2012-07-11 under 510(k) number K121838. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIEBEL-FLARSHEIM DIRECT DIGITAL IMAGING SYSTEM?

LIEBEL-FLARSHEIM DIRECT DIGITAL IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 2012-07-11. The listed applicant is Liebel-Flarsheim. The 510(k) number is K121838.

When did LIEBEL-FLARSHEIM DIRECT DIGITAL IMAGING SYSTEM receive FDA 510(k) clearance?

LIEBEL-FLARSHEIM DIRECT DIGITAL IMAGING SYSTEM received FDA 510(k) clearance on 2012-07-11, under 510(k) number K121838.

Who is the listed applicant for LIEBEL-FLARSHEIM DIRECT DIGITAL IMAGING SYSTEM?

The FDA 510(k) record lists Liebel-Flarsheim as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIEBEL-FLARSHEIM DIRECT DIGITAL IMAGING SYSTEM?

The FDA product code for LIEBEL-FLARSHEIM DIRECT DIGITAL IMAGING SYSTEM is MQB.

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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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