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FDA 510(k)

SYS*STIM 240

K-Number: K113017 · 2012-06-26

ApplicantMettler Electronics Corp.
Decision Date2012-06-26
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SYS*STIM 240 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 2012-06-26 under 510(k) number K113017. 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 240?

SYS*STIM 240 is a medical device that received FDA 510(k) clearance on 2012-06-26. The listed applicant is Mettler Electronics Corp.. The 510(k) number is K113017.

When did SYS*STIM 240 receive FDA 510(k) clearance?

SYS*STIM 240 received FDA 510(k) clearance on 2012-06-26, under 510(k) number K113017.

Who is the listed applicant for SYS*STIM 240?

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 240?

The FDA product code for SYS*STIM 240 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.

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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.

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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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