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FDA 510(k)

CM 3

K-Number: K810348 · 1981-02-23

ApplicantInstrumentation Industries, Inc.
Decision Date1981-02-23
Product CodeCBP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CM 3 is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Industries, Inc.. It received FDA 510(k) clearance on 1981-02-23 under 510(k) number K810348. The device is classified under product code CBP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CM 3?

CM 3 is a medical device that received FDA 510(k) clearance on 1981-02-23. The listed applicant is Instrumentation Industries, Inc.. The 510(k) number is K810348.

When did CM 3 receive FDA 510(k) clearance?

CM 3 received FDA 510(k) clearance on 1981-02-23, under 510(k) number K810348.

Who is the listed applicant for CM 3?

The FDA 510(k) record lists Instrumentation Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CM 3?

The FDA product code for CM 3 is CBP.

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Related Devices (Code: CBP)

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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