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 226

K-Number: K964028 · 1997-02-03

ApplicantMettler Electronics Corp.
Decision Date1997-02-03
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SYS STIM 226 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 1997-02-03 under 510(k) number K964028. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYS STIM 226?

SYS STIM 226 is a medical device that received FDA 510(k) clearance on 1997-02-03. The listed applicant is Mettler Electronics Corp.. The 510(k) number is K964028.

When did SYS STIM 226 receive FDA 510(k) clearance?

SYS STIM 226 received FDA 510(k) clearance on 1997-02-03, under 510(k) number K964028.

Who is the listed applicant for SYS STIM 226?

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 226?

The FDA product code for SYS STIM 226 is IPF.

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.

↑