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FDA 510(k)

CMS 6000

K-Number: K792380 · 1980-01-04

ApplicantPhysio-Control Corp.
Decision Date1980-01-04
Product CodeGYE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CMS 6000 is the device name listed in this FDA 510(k) record. The listed applicant is Physio-Control Corp.. It received FDA 510(k) clearance on 1980-01-04 under 510(k) number K792380. The device is classified under product code GYE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CMS 6000?

CMS 6000 is a medical device that received FDA 510(k) clearance on 1980-01-04. The listed applicant is Physio-Control Corp.. The 510(k) number is K792380.

When did CMS 6000 receive FDA 510(k) clearance?

CMS 6000 received FDA 510(k) clearance on 1980-01-04, under 510(k) number K792380.

Who is the listed applicant for CMS 6000?

The FDA 510(k) record lists Physio-Control Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CMS 6000?

The FDA product code for CMS 6000 is GYE.

Other records listing Physio-Control 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: GYE)

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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