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FDA 510(k)

CC RIDER, MODEL ME180

K-Number: K951916 · 1995-10-04

ApplicantMettler Electronics Corp.
Decision Date1995-10-04
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CC RIDER, MODEL ME180 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 1995-10-04 under 510(k) number K951916. The device is classified under product code IKK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CC RIDER, MODEL ME180?

CC RIDER, MODEL ME180 is a medical device that received FDA 510(k) clearance on 1995-10-04. The listed applicant is Mettler Electronics Corp.. The 510(k) number is K951916.

When did CC RIDER, MODEL ME180 receive FDA 510(k) clearance?

CC RIDER, MODEL ME180 received FDA 510(k) clearance on 1995-10-04, under 510(k) number K951916.

Who is the listed applicant for CC RIDER, MODEL ME180?

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 CC RIDER, MODEL ME180?

The FDA product code for CC RIDER, MODEL ME180 is IKK.

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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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Related Devices (Code: IKK)

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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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