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FDA 510(k)

MODIFIED SONICATOR 720, MODEL ME720

K-Number: K880602 · 1988-02-25

ApplicantMettler Electronics Corp.
Decision Date1988-02-25
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODIFIED SONICATOR 720, MODEL ME720 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 1988-02-25 under 510(k) number K880602. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED SONICATOR 720, MODEL ME720?

MODIFIED SONICATOR 720, MODEL ME720 is a medical device that received FDA 510(k) clearance on 1988-02-25. The listed applicant is Mettler Electronics Corp.. The 510(k) number is K880602.

When did MODIFIED SONICATOR 720, MODEL ME720 receive FDA 510(k) clearance?

MODIFIED SONICATOR 720, MODEL ME720 received FDA 510(k) clearance on 1988-02-25, under 510(k) number K880602.

Who is the listed applicant for MODIFIED SONICATOR 720, MODEL ME720?

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 MODIFIED SONICATOR 720, MODEL ME720?

The FDA product code for MODIFIED SONICATOR 720, MODEL ME720 is IMI.

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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 240K111482SONICATOR PLUS 920K091540MTD 4000K071137SONICATOR PLUS 940, MODEL ME940K053546SONICATOR 740, MODEL ME 740K043586LASER SYS*STIM 540, MODEL ME 540

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Related Devices (Code: IMI)

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K240788Ultrasound StimulatorJkh Health Co., Ltd.K230472Sonopuls 190Enraf-Nonius, B.V.K222098ManaSport+Manamed, Inc.K210284ManaSportManamed, Inc.K202788Sonomed IV, Sonomed VCarci Industria E Comercio DE Aparelhos Cirurgicos E OrtoK160378BRH-A2 Combined Ultrasound and Electric Field Stimulation (CUSEFS)Brh Medical , 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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