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FDA 510(k)

MIDIFICATION SYS*STIM 207 (MODEL-ME207)

K-Number: K855249 · 1986-03-28

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

Device Summary

MIDIFICATION SYS*STIM 207 (MODEL-ME207) 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 K855249. 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 MIDIFICATION SYS*STIM 207 (MODEL-ME207)?

MIDIFICATION SYS*STIM 207 (MODEL-ME207) 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 K855249.

When did MIDIFICATION SYS*STIM 207 (MODEL-ME207) receive FDA 510(k) clearance?

MIDIFICATION SYS*STIM 207 (MODEL-ME207) received FDA 510(k) clearance on 1986-03-28, under 510(k) number K855249.

Who is the listed applicant for MIDIFICATION SYS*STIM 207 (MODEL-ME207)?

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 MIDIFICATION SYS*STIM 207 (MODEL-ME207)?

The FDA product code for MIDIFICATION SYS*STIM 207 (MODEL-ME207) is IPF.

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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: 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.

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