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FDA 510(k)

SONICATOR PLUS 920

K-Number: K111482 · 2011-08-25

ApplicantMettler Electronics Corp.
Decision Date2011-08-25
Product CodeIMG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SONICATOR PLUS 920 is the device name listed in this FDA 510(k) record. The listed applicant is Mettler Electronics Corp.. It received FDA 510(k) clearance on 2011-08-25 under 510(k) number K111482. The device is classified under product code IMG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONICATOR PLUS 920?

SONICATOR PLUS 920 is a medical device that received FDA 510(k) clearance on 2011-08-25. The listed applicant is Mettler Electronics Corp.. The 510(k) number is K111482.

When did SONICATOR PLUS 920 receive FDA 510(k) clearance?

SONICATOR PLUS 920 received FDA 510(k) clearance on 2011-08-25, under 510(k) number K111482.

Who is the listed applicant for SONICATOR PLUS 920?

The FDA 510(k) record lists Mettler Electronics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SONICATOR PLUS 920?

The FDA product code for SONICATOR PLUS 920 is IMG.

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Other records listing Mettler Electronics Corp. as applicant

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.

K113017SYS*STIM 240K091540MTD 4000K071137SONICATOR PLUS 940, MODEL ME940K053546SONICATOR 740, MODEL ME 740K043586LASER SYS*STIM 540, MODEL ME 540K042554AUTO THERM 390, MODEL ME 390

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Related Devices (Code: IMG)

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.

K244041Ultrasound Therapy Workstation (XMS-UET2)Xemis Medical Technology (Shenzhen) Co., Ltd.K153559OmniVersa Multi-Modality Therapy System and Omnistim FX2 Professional Therapy SystemAccelerated Care Plus (Acp)K120217SONICSTIMU COMBO THERAPEUTIC DEVICEShenzhen Dongdixin Technology Co., Ltd.K121059SOLEOLINE, SOLEO STIM, SOLEO SONO, SOLEO SONOSTIMZimmer Medizinsystems GmbHK102524FUTURADr. Oliver Wenker, M.D., M.B.A.K102190WINSTIMJohari Digital Healthcare , 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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