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FDA 510(k)

EMS PIEZON MASTER SURGERY

K-Number: K072146 · 2007-12-18

ApplicantE.M.S Electro Medical Systems S.A
Decision Date2007-12-18
Product CodeDZI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EMS PIEZON MASTER SURGERY is the device name listed in this FDA 510(k) record. The listed applicant is E.M.S Electro Medical Systems S.A. It received FDA 510(k) clearance on 2007-12-18 under 510(k) number K072146. The device is classified under product code DZI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMS PIEZON MASTER SURGERY?

EMS PIEZON MASTER SURGERY is a medical device that received FDA 510(k) clearance on 2007-12-18. The listed applicant is E.M.S Electro Medical Systems S.A. The 510(k) number is K072146.

When did EMS PIEZON MASTER SURGERY receive FDA 510(k) clearance?

EMS PIEZON MASTER SURGERY received FDA 510(k) clearance on 2007-12-18, under 510(k) number K072146.

Who is the listed applicant for EMS PIEZON MASTER SURGERY?

The FDA 510(k) record lists E.M.S Electro Medical Systems S.A as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMS PIEZON MASTER SURGERY?

The FDA product code for EMS PIEZON MASTER SURGERY is DZI.

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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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