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FDA 510(k)

EMS PIEZON MASTER 700

K-Number: K093000 · 2010-07-30

ApplicantE.M.S Electro Medical Systems S.A
Decision Date2010-07-30
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EMS PIEZON MASTER 700 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 2010-07-30 under 510(k) number K093000. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMS PIEZON MASTER 700?

EMS PIEZON MASTER 700 is a medical device that received FDA 510(k) clearance on 2010-07-30. The listed applicant is E.M.S Electro Medical Systems S.A. The 510(k) number is K093000.

When did EMS PIEZON MASTER 700 receive FDA 510(k) clearance?

EMS PIEZON MASTER 700 received FDA 510(k) clearance on 2010-07-30, under 510(k) number K093000.

Who is the listed applicant for EMS PIEZON MASTER 700?

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 700?

The FDA product code for EMS PIEZON MASTER 700 is ELC.

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Other records listing E.M.S Electro Medical Systems S.A as applicant

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Related Devices (Code: ELC)

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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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