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FDA 510(k)

MASTERTORQUE LUX 8900 L

K-Number: K130560 · 2013-09-27

ApplicantKaltenbach & Voigt GmbH
Decision Date2013-09-27
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MASTERTORQUE LUX 8900 L is the device name listed in this FDA 510(k) record. The listed applicant is Kaltenbach & Voigt GmbH. It received FDA 510(k) clearance on 2013-09-27 under 510(k) number K130560. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASTERTORQUE LUX 8900 L?

MASTERTORQUE LUX 8900 L is a medical device that received FDA 510(k) clearance on 2013-09-27. The listed applicant is Kaltenbach & Voigt GmbH. The 510(k) number is K130560.

When did MASTERTORQUE LUX 8900 L receive FDA 510(k) clearance?

MASTERTORQUE LUX 8900 L received FDA 510(k) clearance on 2013-09-27, under 510(k) number K130560.

Who is the listed applicant for MASTERTORQUE LUX 8900 L?

The FDA 510(k) record lists Kaltenbach & Voigt GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MASTERTORQUE LUX 8900 L?

The FDA product code for MASTERTORQUE LUX 8900 L is EFB.

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Related Devices (Code: EFB)

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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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