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FDA 510(k)

FEMTO LDV

K-Number: K112154 · 2012-03-16

ApplicantSie Ag,Surgical Instument Engineering
Decision Date2012-03-16
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FEMTO LDV is the device name listed in this FDA 510(k) record. The listed applicant is Sie Ag,Surgical Instument Engineering. It received FDA 510(k) clearance on 2012-03-16 under 510(k) number K112154. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FEMTO LDV?

FEMTO LDV is a medical device that received FDA 510(k) clearance on 2012-03-16. The listed applicant is Sie Ag,Surgical Instument Engineering. The 510(k) number is K112154.

When did FEMTO LDV receive FDA 510(k) clearance?

FEMTO LDV received FDA 510(k) clearance on 2012-03-16, under 510(k) number K112154.

Who is the listed applicant for FEMTO LDV?

The FDA 510(k) record lists Sie Ag,Surgical Instument Engineering as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FEMTO LDV?

The FDA product code for FEMTO LDV is HQF.

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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.

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