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FDA 510(k)

SYS*STIM 220

K-Number: K883080 · 1989-04-27

ApplicantMettler Electronics Corp.
Decision Date1989-04-27
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SYS*STIM 220 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 1989-04-27 under 510(k) number K883080. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYS*STIM 220?

SYS*STIM 220 is a medical device that received FDA 510(k) clearance on 1989-04-27. The listed applicant is Mettler Electronics Corp.. The 510(k) number is K883080.

When did SYS*STIM 220 receive FDA 510(k) clearance?

SYS*STIM 220 received FDA 510(k) clearance on 1989-04-27, under 510(k) number K883080.

Who is the listed applicant for SYS*STIM 220?

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 220?

The FDA product code for SYS*STIM 220 is LIH.

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.

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Related Devices (Code: LIH)

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.

K231575Vecttor VT-300Artaflex, Inc.K202725ETD4000Therasigma, LLCK183692Avid IF2Vision Quest Industries Inc./Dba VQ OrthocareK122944GEMORE TRUE SINE INTERFERENTIAL STIMULATORGemore Technology Co, Ltd.K121662VECTTOR VT-200Alan Neuromedical Technologies, LLCK110509EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908Everyway Medical Instruments 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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