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FDA 510(k)

SYS STIM 206 MODEL ME206

K-Number: K851735 · 1985-11-19

ApplicantMettler Electronics Corp.
Decision Date1985-11-19
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SYS STIM 206 MODEL ME206 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 1985-11-19 under 510(k) number K851735. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYS STIM 206 MODEL ME206?

SYS STIM 206 MODEL ME206 is a medical device that received FDA 510(k) clearance on 1985-11-19. The listed applicant is Mettler Electronics Corp.. The 510(k) number is K851735.

When did SYS STIM 206 MODEL ME206 receive FDA 510(k) clearance?

SYS STIM 206 MODEL ME206 received FDA 510(k) clearance on 1985-11-19, under 510(k) number K851735.

Who is the listed applicant for SYS STIM 206 MODEL ME206?

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 206 MODEL ME206?

The FDA product code for SYS STIM 206 MODEL ME206 is GZJ.

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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.

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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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