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FDA 510(k)

SYS STIM 294, MODEL ME 294

K-Number: K984114 · 1999-02-09

ApplicantMettler Electronics Corp.
Decision Date1999-02-09
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SYS STIM 294, MODEL ME 294 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 1999-02-09 under 510(k) number K984114. 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 294, MODEL ME 294?

SYS STIM 294, MODEL ME 294 is a medical device that received FDA 510(k) clearance on 1999-02-09. The listed applicant is Mettler Electronics Corp.. The 510(k) number is K984114.

When did SYS STIM 294, MODEL ME 294 receive FDA 510(k) clearance?

SYS STIM 294, MODEL ME 294 received FDA 510(k) clearance on 1999-02-09, under 510(k) number K984114.

Who is the listed applicant for SYS STIM 294, MODEL ME 294?

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 294, MODEL ME 294?

The FDA product code for SYS STIM 294, MODEL ME 294 is IPF.

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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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