Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SONICATOR 740, MODEL ME 740

K-Number: K053546 · 2006-05-04

ApplicantMettler Electronics Corp.
Decision Date2006-05-04
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SONICATOR 740, MODEL ME 740 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 2006-05-04 under 510(k) number K053546. 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 SONICATOR 740, MODEL ME 740?

SONICATOR 740, MODEL ME 740 is a medical device that received FDA 510(k) clearance on 2006-05-04. The listed applicant is Mettler Electronics Corp.. The 510(k) number is K053546.

When did SONICATOR 740, MODEL ME 740 receive FDA 510(k) clearance?

SONICATOR 740, MODEL ME 740 received FDA 510(k) clearance on 2006-05-04, under 510(k) number K053546.

Who is the listed applicant for SONICATOR 740, MODEL ME 740?

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 740, MODEL ME 740?

The FDA product code for SONICATOR 740, MODEL ME 740 is IMI.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 ME940K043586LASER SYS*STIM 540, MODEL ME 540K042554AUTO THERM 390, MODEL ME 390

View all 32 devices →

Related Devices (Code: IMI)

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.

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.

↑