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FDA 510(k)

NCS FISH-FIT MD SYSTEM FISH-FIT MD COMPASS MD

K-Number: K120356 · 2012-12-11

ApplicantNcs Lab Srl
Decision Date2012-12-11
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NCS FISH-FIT MD SYSTEM FISH-FIT MD COMPASS MD is the device name listed in this FDA 510(k) record. The listed applicant is Ncs Lab Srl. It received FDA 510(k) clearance on 2012-12-11 under 510(k) number K120356. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NCS FISH-FIT MD SYSTEM FISH-FIT MD COMPASS MD?

NCS FISH-FIT MD SYSTEM FISH-FIT MD COMPASS MD is a medical device that received FDA 510(k) clearance on 2012-12-11. The listed applicant is Ncs Lab Srl. The 510(k) number is K120356.

When did NCS FISH-FIT MD SYSTEM FISH-FIT MD COMPASS MD receive FDA 510(k) clearance?

NCS FISH-FIT MD SYSTEM FISH-FIT MD COMPASS MD received FDA 510(k) clearance on 2012-12-11, under 510(k) number K120356.

Who is the listed applicant for NCS FISH-FIT MD SYSTEM FISH-FIT MD COMPASS MD?

The FDA 510(k) record lists Ncs Lab Srl as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NCS FISH-FIT MD SYSTEM FISH-FIT MD COMPASS MD?

The FDA product code for NCS FISH-FIT MD SYSTEM FISH-FIT MD COMPASS MD is MBI.

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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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