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)

SYS*STIM 206 (MODEL-ME 206)

K-Number: K860107 · 1986-03-28

ApplicantMettler Electronics Corp.
Decision Date1986-03-28
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

SYS*STIM 206 (MODEL-ME 206) 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 1986-03-28 under 510(k) number K860107. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the SYS*STIM 206 (MODEL-ME 206)?

SYS*STIM 206 (MODEL-ME 206) is a medical device that received FDA 510(k) clearance on 1986-03-28. The listed applicant is Mettler Electronics Corp.. The 510(k) number is K860107.

When did SYS*STIM 206 (MODEL-ME 206) receive FDA 510(k) clearance?

SYS*STIM 206 (MODEL-ME 206) received FDA 510(k) clearance on 1986-03-28, under 510(k) number K860107.

Who is the listed applicant for SYS*STIM 206 (MODEL-ME 206)?

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 SYS*STIM 206 (MODEL-ME 206)?

The FDA product code for SYS*STIM 206 (MODEL-ME 206) is IPF.

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 ME940K053546SONICATOR 740, MODEL ME 740K043586LASER SYS*STIM 540, MODEL ME 540

View all 32 devices →

Related Devices (Code: IPF)

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.

K253542Apollo Quattro (APQ-10M)Weero Co., Ltd.K252816High Tone Power therapy (HiToP) (Model: HiToP PNP)Mohammadali NezakatiK260142StimelMD (SSMD) systemMotion Informatics ltd.K251083Compact IIEnraf-Nonius, B.V.K241433EVE Synergy (EVE-20M)Weero Co., Ltd.K241488TrainFES AdvanceTrainfes

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.

↑