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FDA 510(k)

EMS AIR-FLOW MASTER PIEZON

K-Number: K110173 · 2011-04-07

ApplicantE.M.S Electro Medical Systems S.A
Decision Date2011-04-07
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EMS AIR-FLOW MASTER PIEZON 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 2011-04-07 under 510(k) number K110173. 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 AIR-FLOW MASTER PIEZON?

EMS AIR-FLOW MASTER PIEZON is a medical device that received FDA 510(k) clearance on 2011-04-07. The listed applicant is E.M.S Electro Medical Systems S.A. The 510(k) number is K110173.

When did EMS AIR-FLOW MASTER PIEZON receive FDA 510(k) clearance?

EMS AIR-FLOW MASTER PIEZON received FDA 510(k) clearance on 2011-04-07, under 510(k) number K110173.

Who is the listed applicant for EMS AIR-FLOW MASTER PIEZON?

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 AIR-FLOW MASTER PIEZON?

The FDA product code for EMS AIR-FLOW MASTER PIEZON 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)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260773Varios Combi Pro2Nakanishi, Inc.K253254GBT Machine Airflow Prophylaxis MasterE.M.S Electro Medical Systems S.AK251689VARIOS 170 LUX SCALER SYSTEM (VA170LUXS10); VARIOS 170 LUX SCALER SYSTEM (VA170LUXS11); VARIOS 170 SCALER SYSTEM (VA170S11)Nakanishi, Inc.K242317Integrated Endo System (Meet Endo-II)Denjoy Dental Co., Ltd.K233844OdneCleanOdne AGK240707Ultrasonic Scaler (WD-JY-B002,WD-JY-W001,WD-JY-R003,WD-JY-G004,WD-JY-B003,WD-JY-C006,WD-JY-M0014, WD-JY-N0015,WD-JY-N0016,WD-JY-N0017,WD-JY-E007, WD-JY-F008,WD-JY-A005,WD-JY-H009,WD-JY-I0011, WD-JY-K0012,WD-JY-K0013,WD-JY-K0014, WD-JY-L0013,WD-JY-L0014,WD-JY-L0015, WD-JY-L0016,WD-JY-L0017)Shenzhen Micro Electric Intelligence Co., Ltd.

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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